- a.Penicillin
- b.Ceftriaxone
- c.Tetracycline
- d.Interferon alpha
- e.Erythromycin

Custom Search
Showing posts with label INFECTION. Show all posts
Showing posts with label INFECTION. Show all posts
Treatment of choice for a case of secondary syphilis
A 20-year-old student has a macular rash, generalized lymphadenopathy, apthous ulcers, and gray-white plaques around the anal area. A dark-field examination demonstrates spirochetes. Which of the following is the treatment of choice for this patient?
The answer is a.
Penicillin is the drug of choice for secondary syphilis. A positive darkfield examination in this patient confirms the diagnosis."benzathine penicillin G 2.4 million units IM or aqueous procaine penicillin G 600,000 units IM daily for ten days-In Late latent (more than 2 years), and tertiary syphilis treatment is benzathine penicillin G 2.4 million units weekly for three weeks or aqueous procaine penicillin G 600,000 units daily for 15 days.".
Ceftriaxone and tetracycline are usually considered to be alternative therapies. Interferon alpha has been used in the treatment of condyloma acuminata, a lesion that can be mistaken for syphilitic condyloma.
A case of Chromoblastomycosis
A 55-year-old man presented with vegetating lesions on the right foot that had been slowly enlarging during the past several years ;The photo:
On physical examination, several nodular and verrucous lesions were seen in the distal region of the foot. The patient lived in a rural area and had walked barefoot for most of his life. Analysis of a skin-biopsy specimen revealed clusters of small, round, thick-walled, brown sclerotic bodies in the stratum corneum (muriform cells), which are diagnostic for chromoblastomycosis.
Chromoblastomycosis is a chronic, soft-tissue fungal infection commonly caused by Fonsecaea pedrosoi, Phialophora verrucosa, Cladosporium carrionii, or F. compacta. The infection occurs in tropical or subtropical climates and often in rural areas. The fungi are usually introduced to the skin through cutaneous injury from thorns, splinters, or other plant debris. The patient was treated with multiple surgical excisions and itraconazole for 24 months with a complete resolution of symptoms.
On physical examination, several nodular and verrucous lesions were seen in the distal region of the foot. The patient lived in a rural area and had walked barefoot for most of his life. Analysis of a skin-biopsy specimen revealed clusters of small, round, thick-walled, brown sclerotic bodies in the stratum corneum (muriform cells), which are diagnostic for chromoblastomycosis.
Chromoblastomycosis is a chronic, soft-tissue fungal infection commonly caused by Fonsecaea pedrosoi, Phialophora verrucosa, Cladosporium carrionii, or F. compacta. The infection occurs in tropical or subtropical climates and often in rural areas. The fungi are usually introduced to the skin through cutaneous injury from thorns, splinters, or other plant debris. The patient was treated with multiple surgical excisions and itraconazole for 24 months with a complete resolution of symptoms.
Chickenpox infection
A 25 years old teacher develops fever and an itchy rash over her face and chest. on exam : multiple papules and vesicles in varying stages of development. 1 week later she complains of cough and is found to have an infiltrate on x-ray.the most likely etiology of the infection?
- a. Streptococcus pneumoniae
- b. Mycoplasma pneumoniae
- c. Pneumocystis carinii
- d. Varicella virus
- e. Chlamydia psitacii
The answer is d.
Varicella pneumonia develops in about 20% of adults with chickenpox. It occurs 3 to 7 days after the onset of the rash. The hallmark of the chickenpox rash is papules, vesicles, and scabs in various stages of development. Fever, malaise, and itching are usually part of the clinical picture. The differential can include some coxsackievirus and echovirus infections, which might present with pneumonia and vesicular rash. Rickettsialpox, a rickettsial infection, has also been mistaken for chickenpox.
Clinical symptoms of Haemophilus influenzae Vs Haemophilus ducreyi Vs Haemophilus aegyptius
Haemophilus influenzae
H. influenzae has a variety of symptoms some of which may depend on the presence of the bacterial capsule. Until the availability of the Hib vaccine, the type-b H. influenzae was the main cause of meningitis in children between 6 months and 5 years, although older children, adolescents and adults can also be infected. At first the infection causes a runny nose, low grade fever and headache (1-3 days). Due to the invasive nature of the organism ,it enters the circulation and crosses the blood-brain barrier, resulting in a rapidly progressing meningitis (stiff neck), convulsions, coma and death. Timely treatment may prevent coma and death, but the patient may still suffer from deafness and mental retardation.
Type-b H. influenzae may also cause septic arthritis conjunctivitis, cellulitis, and epiglottitis, the latter results in the obstruction of the upper airway and suffocation. H. influenzae of other types may rarely cause some of the symptoms listed above.
Non-typable strains of H. influenzae are the second commonest cause of otitis media in young children (second to Streptococcus pneumoniae). In adults, these organisms cause pneumonia, particularly in individuals with other underlying pulmonary infections. These organisms also cause acute or chronic sinusitis in individuals of all ages.
Clinical symptoms of infection by HaemophilusClinical symptoms of infection by HaemophilusClinical symptoms of infection by Haemophilus
Haemophilus ducreyi
A significant cause of genital ulcers (chancroid) in Asia and Africa but, is seen less commonly in the USA. The incidence is approximately 4000-5000 per year with clusters found in California, Florida, Georgia and New York. The infection is asymptomatic in women but about a week following sexual transmission to a man, it causes appearance of a tender papule with erythematous base on the genitalia or the peripheral area. The lesion progresses to become a painful ulcer with inguinal lymphadenopathy. The H. ducreyi lesion (chancroid) is distinguished from a syphilitic lesion (chancre) in that it is a comparatively soft lesion.
Haemophilus influenzae aegyptius
This bacterium, previously known as H. aegyptius, causes an opportunistic organism which can result in a fulminant pediatric disease (Brazilian purpuric fever) characterized by an initial conjunctivitis, followed by an acute onset of fever, accompanied by vomiting and abdominal pain. Subsequently, the patient develops petechiae, purpura, shock and may face death. The pathogenesis of this infection is poorly understood. The growth conditions for this organism are the same as those for H. influenzae.
Ramsay Hunt Syndrome(clinical)
CAUSES:
Classic Ramsay Hunt syndrome is ascribed to infection of the geniculate ganglion by herpesvirus 3 (varicella-zoster virus [VZV]).

HISTORY:
*Patients usually present with paroxysmal pain deep within the ear. The pain often radiates outward into the pinna of the ear and may be associated with a more constant, diffuse, and dull background pain.
*The onset of pain usually precedes the rash by several hours and even days.
*Classic Ramsay Hunt syndrome can be associated with the following:
-Vesicular rash of the ear or mouth (as many as 83% of cases),The rash might precede the onset of facial paresis/palsy.
-Ipsilateral lower motor neuron facial paresis/palsy (CN VII)
-Vertigo and ipsilateral hearing loss (CN VII)
-Tinnitus,Otalgia,Headaches,DysarthriaGait,ataxia.
-Fever,Cervical adenopathy.
*Facial weakness usually reaches maximum severity by one week after the onset of symptoms.
*Other cranial neuropathies might be present and may involve cranial nerves (CNs) VIII, IX, X, V, and VI.
*Ipsilateral hearing loss has been reported in as many as 50% of cases.
*Blisters of the skin of the ear canal, auricle, or both may become secondarily infected, causing cellulitis.
EXAMINATION:
.The primary physical findings in classic Ramsay Hunt syndrome include peripheral facial nerve paresis with associated rash or herpetic blisters in the distribution of the nervus intermedius.
.The location of the accompanying rash varies from patient to patient, as does the area innervated by the nervus intermedius. It may include the following:
1.Anterior two thirds of the tongue
2.Soft palate
3.External auditory canal
4.Pinna
.The patient may have associated ipsilateral hearing loss and balance problems.
.A thorough physical examination must be performed, including neuro-otologic and audiometric assessment.
Classic Ramsay Hunt syndrome is ascribed to infection of the geniculate ganglion by herpesvirus 3 (varicella-zoster virus [VZV]).

HISTORY:
*Patients usually present with paroxysmal pain deep within the ear. The pain often radiates outward into the pinna of the ear and may be associated with a more constant, diffuse, and dull background pain.
*The onset of pain usually precedes the rash by several hours and even days.
*Classic Ramsay Hunt syndrome can be associated with the following:
-Vesicular rash of the ear or mouth (as many as 83% of cases),The rash might precede the onset of facial paresis/palsy.
-Ipsilateral lower motor neuron facial paresis/palsy (CN VII)
-Vertigo and ipsilateral hearing loss (CN VII)
-Tinnitus,Otalgia,Headaches,DysarthriaGait,ataxia.
-Fever,Cervical adenopathy.
*Facial weakness usually reaches maximum severity by one week after the onset of symptoms.
*Other cranial neuropathies might be present and may involve cranial nerves (CNs) VIII, IX, X, V, and VI.
*Ipsilateral hearing loss has been reported in as many as 50% of cases.
*Blisters of the skin of the ear canal, auricle, or both may become secondarily infected, causing cellulitis.
EXAMINATION:
.The primary physical findings in classic Ramsay Hunt syndrome include peripheral facial nerve paresis with associated rash or herpetic blisters in the distribution of the nervus intermedius.
.The location of the accompanying rash varies from patient to patient, as does the area innervated by the nervus intermedius. It may include the following:
1.Anterior two thirds of the tongue
2.Soft palate
3.External auditory canal
4.Pinna
.The patient may have associated ipsilateral hearing loss and balance problems.
.A thorough physical examination must be performed, including neuro-otologic and audiometric assessment.
Toxoplasmosis in Immune-Suppressed Patients
Toxoplasma encephalitis (inflammation of the brain) and Toxoplasma myocarditis (inflammation of the heart) are well recognised opportunistic infections in patients who are immune suppressed, particularly in relation to AIDS and chemotherapy for cancer. The Toxoplasma encephalitis has the usual appearance of an encephalitis from any cause, that is, focal areas of death of cerebral tissue associated with a mononuclear inflammatory cell infiltrate. But in addition, Toxoplasma cysts are found in the affected brain tissue.
This figures are from the heart of a middle aged male who died from AIDS. The Toxoplasma cyst is expanding the myocardial muscle fibre. In this case there is no inflammatory reaction associated with the cyst. The presence of an inflammatory reaction is variable.
This figures are from the heart of a middle aged male who died from AIDS. The Toxoplasma cyst is expanding the myocardial muscle fibre. In this case there is no inflammatory reaction associated with the cyst. The presence of an inflammatory reaction is variable.
Diplopia in a Patient with HIV Infection

A 25-year-old man with human immunodeficiency virus (HIV) infection who was receiving highly active antiretroviral therapy presented with a 1-week history of diplopia and headache. The CD4 count was 218 cells per cubic millimeter, and the viral load was 50,000 copies per milliliter.
The neurologic examination revealed an inability to abduct the right eye with horizontal gaze, a finding that was consistent with an isolated right abducens nerve palsy (rightward gaze, Panel A; leftward gaze, Panel B). The examination of other cranial nerves was normal. The remainder of the motor and sensory examination was within normal limits.
The patient reported having had low back pain and constipation for the previous week. There was no history of bowel or bladder incontinence. A gadolinium-enhanced magnetic resonance image of the brain showed a minimally enhancing mass filling and expanding the right cavernous sinus (Panel C, arrow). Lumbar-spine imaging showed a mass with similar radiographic characteristics involving the ventral epidural compartment.
Biopsy of the spinal lesion revealed diffuse large-B-cell lymphoma. A chemotherapeutic regimen of cyclophosphamide, doxorubicin, vincristine, and prednisolone, along with the monoclonal antibody rituximab (R-CHOP), was started. Progressive leg weakness from spinal involvement developed, and the patient had a poor response to corticosteroids and radiation therapy and died 3 months later.
Fournier's Gangrene Reconstructed By Pedicle Thigh Flap(step by step photo images)

Fournier's gangrene is a rare condition and delayed treatment results in fatal outcome. We managed a case of Fournier's gangrene by initial radical debridement followed by scrotal reconstruction using pedicle thigh flap to cover the bare testes with excellent results.

35-year-old male presented in the emergency department with the swelling over scrotum and watery discharge from the left side of the scrotum. Initially he developed a small swelling at the root of one of hair on the left side of the scrotum. Gradually the area around the swelling became red, painful and hard. The redness, swelling and the pain spread over whole of the scrotum within 2 days and the affected hair follicle started discharging watery fluid. Patient became feverish, dull and pale. On examination, there was gross involvement of the scrotum, which was swollen, inflamed and severely tender on touch (Figure1).

On examination there was gross thickening of the scrotal skin and testis were not palpable. Ultrasonography showed a scrotal wall thickening of 1 cm with collection of hyper echoic fluid around the testes. Doppler showed normal blood supply to both the testes.
Patient shifted to emergency operation theater and whole of the infected scrotal wall debrided exposing the testes. Daily dressing done with povidone iodine for 9 days after which the testes covered with the healthy granulation tissue (Figure 2).
On the 9th day in the elective surgery, after preparing the wound, excess granulation tissue scraped from the testes. The pedicle fascio cutaneous flaps developed from the femoral triangle on both the side as shown in the figure 3 by sharp dissection by using bipolar cautary.

The flaps rotated and tied over the bare testes in the midline and fixed with staples. Then the upper margins of the flaps fixed to the upper margin of the raw area finally followed by the lower margin. Flaps rotated and placed without tension with corrugated drains underneath. (Figure 4).

The area left behind on the femoral triangles on both the thighs due to the rotation of the flaps covered with split thickness skin graft taken from the lower anterior portion of the right thigh (Figure 5).

The drains were removed on the third postoperative day. The flaps were taken up well and the spit thickness skin graft uptake over the residual raw area were good. The patient sent home on tenth day and was under follow up lately until last 1 year without any complications.
TB and STAFF
BCG vaccination will be offered to healthcare workers, irrespective of age, who fulfil all the following criteria:
1. previously unvaccinated (that is, without adequate documentation or a characteristic scar)
2. will have contact with patients or clinical materials.
3. are Mantoux (or interferon-gamma test for latent tuberculosis) negative.
All staff in contact with patients with smear positive pulmonary tuberculosis should be aware of the following principles.
-The importance of BCG immunisation as a basic protection
-The need to report to Occupational Health or senior ward staff if they are unusually susceptible e.g. transplant recipient taking immunosuppressive therapy, HIV positive.
-The extremely low risk of occupationally acquired tuberculosis where appropriate precautions are taken.
-The need to report any symptoms suggestive of tuberculosis to the Occupational
Health Department.
Staff in contact with open pulmonary tuberculosis do not normally need follow up. A decision on this will be made by the Occupational Health Department in conjunction with a Consultant Microbiologist or Consultant Respiratory Physician.
1. previously unvaccinated (that is, without adequate documentation or a characteristic scar)
2. will have contact with patients or clinical materials.
3. are Mantoux (or interferon-gamma test for latent tuberculosis) negative.
All staff in contact with patients with smear positive pulmonary tuberculosis should be aware of the following principles.
-The importance of BCG immunisation as a basic protection
-The need to report to Occupational Health or senior ward staff if they are unusually susceptible e.g. transplant recipient taking immunosuppressive therapy, HIV positive.
-The extremely low risk of occupationally acquired tuberculosis where appropriate precautions are taken.
-The need to report any symptoms suggestive of tuberculosis to the Occupational
Health Department.
Staff in contact with open pulmonary tuberculosis do not normally need follow up. A decision on this will be made by the Occupational Health Department in conjunction with a Consultant Microbiologist or Consultant Respiratory Physician.
Mucormycosis
A 44-year-old woman with a 20-year history of poorly controlled diabetes mellitus presents with headache and unilateral proptosis. The patient is febrile and appears toxic. Her serum glucose level is 640 mg/dL. An urgent CT scan of the head reveals a retroorbital abscess and severe opacification of the frontal and ethmoid sinuses.
Which of the following organisms is most likely responsible for this infection?
The answer is (b).
Mucormycosis is a rare fungal disease (Rhizopus species are the most common causative organisms ) limited to persons with preexisting illness and may be seen in poorly controlled diabetic patients. Severe infection of the facial sinuses, which may extend into the brain, is the most common presentation. Patients present with fever, nasalcongestion, sinus pain, diplopia, and coma.
Physical examination may reveal a necrotic nasal turbinate, reduced ocular motion, proptosis, and blindness. CT scan or MRI will reveal the extent of sinus involvement prior to surgery.
Which of the following organisms is most likely responsible for this infection?
- a. Cryptococcus neoformans
- b. Mucormycosis
- c. Mycobacterium tuberculosis
- d. Toxoplasma gondii
- e. Listeria monocytogenes
- f. Staphylococcus epidermis
The answer is (b).
Mucormycosis is a rare fungal disease (Rhizopus species are the most common causative organisms ) limited to persons with preexisting illness and may be seen in poorly controlled diabetic patients. Severe infection of the facial sinuses, which may extend into the brain, is the most common presentation. Patients present with fever, nasalcongestion, sinus pain, diplopia, and coma.
Physical examination may reveal a necrotic nasal turbinate, reduced ocular motion, proptosis, and blindness. CT scan or MRI will reveal the extent of sinus involvement prior to surgery.
Postmortem photograph of a woman with diabetes and left rhinocerebral mucormycosis complicating ketoacidosis. Rhizopus oryzae was the causative organism. Note the orbital and facial cellulitis and the black nasal discharge. (Courtesy of A. Allworth, MD, Brisbane, Australia)
Ramsay Hunt Syndrome
What is it? Ramsay Hunt syndrome is defined as an acute peripheral facial neuropathy associated with erythematous vesicular rash of the skin of the ear canal, auricle (also termed herpes zoster oticus,Hunt's Syndrome ), and/or mucous membrane of the oropharynx.
This syndrome is also known as geniculate neuralgia or nervus intermedius neuralgia. Ramsay Hunt syndrome can also occur in the absence of a skin rash, condition known as zoster sine herpete.
VZV infection causes 2 distinct clinical syndromes. Primary infection, also known as varicella or chickenpox, is a common pediatric erythematous disease characterized by a highly contagious generalized vesicular rash. The annual incidence of varicella infection has significantly declined after the introduction of mass vaccination programs in most countries of the world. After chickenpox, VZV remain latent in neurons of cranial nerve and dorsal root ganglia. Subsequent reactivation of latent VZV can result in localized vesicular rash, known as herpes zoster. VZV infection or reactivation involving the geniculate ganglion of CN VII within the temporal bone is the main pathophysiological mechanism of Ramsay Hunt syndrome.
This syndrome is also known as geniculate neuralgia or nervus intermedius neuralgia. Ramsay Hunt syndrome can also occur in the absence of a skin rash, condition known as zoster sine herpete.
Pathophysiology:
Ramsay Hunt syndrome is defined as VZV infection of the head and neck that involves the facial nerve, often the seventh cranial nerve (CN VII). Other cranial nerves might be also involved, including CN VIII, IX, V, and VI (in order of frequency). This infection gives rise to vesiculation and ulceration of the external ear and ipsilateral anterior two thirds of the tongue and soft palate, as well as ipsilateral facial neuropathy (in CN VII), radiculoneuropathy, or geniculate ganglionopathy. VZV infection causes 2 distinct clinical syndromes. Primary infection, also known as varicella or chickenpox, is a common pediatric erythematous disease characterized by a highly contagious generalized vesicular rash. The annual incidence of varicella infection has significantly declined after the introduction of mass vaccination programs in most countries of the world. After chickenpox, VZV remain latent in neurons of cranial nerve and dorsal root ganglia. Subsequent reactivation of latent VZV can result in localized vesicular rash, known as herpes zoster. VZV infection or reactivation involving the geniculate ganglion of CN VII within the temporal bone is the main pathophysiological mechanism of Ramsay Hunt syndrome.
Mortality/Morbidity:
Ramsay Hunt syndrome is not usually associated with mortality. It is a self-limiting disease; the primary morbidity results from facial weakness. Unlike Bell palsy, this syndrome has a complete recovery rate of less than 50%.
SYMPTOMS OF MALARIA
Sometimes symptoms of malaria infection are not always dramatic, and can easily be dismissed as unimportant.

Plasmodium falciparum normally take 7 to 14 days to show symptoms while Plasmodium vivax and ovale normally take 8 to 14 days (but in some cases can survive for some months in the human horst) and Plasmodium malariae 7 to 30 days.
Symptoms may appear and disappear in phases and may come and go at various time frames. These cyclic symptoms of malaria are caused by the life cycle of the parasites - as they develop, mature, reproduce and are once again released into the blood stream to infect even more blood and liver cells.

Plasmodium falciparum normally take 7 to 14 days to show symptoms while Plasmodium vivax and ovale normally take 8 to 14 days (but in some cases can survive for some months in the human horst) and Plasmodium malariae 7 to 30 days.
Symptoms may appear and disappear in phases and may come and go at various time frames. These cyclic symptoms of malaria are caused by the life cycle of the parasites - as they develop, mature, reproduce and are once again released into the blood stream to infect even more blood and liver cells.
Recommendations for post-sexual exposure HIV prophylaxis

Post exposure HIV prophylaxis is recommended if there is:-
* unprotected receptive anal intercourse
* unprotected receptive vaginal intercourse
* unprotected insertive vaginal intercourse
* unprotected insertive anal intercourse
* unprotected receptive fellatio with ejaculation
with a HIV positive person or if the person is a HIV risk group (gay or bisexual men, injection drug users or sex workers), and if the exposure is isolated and the patient is commited to safer sex in the future and the exposure occurred within 72 hours of presentation for care.
Exposure to persons known to be HIV infected
- if medication regimen of source patient is unknown => prescribe Zivudine (AZT/ZDV) 300mg bid + Lamivudine (Epivir) 150mg bid + Indinavir (Crixivan) 800mh q8h or nelfinavir (Virasept) 1250mg bid or 750mg tid
- Combivir 1 tablet bid may be substituted for zidovudine and lamivudine
- if medication regimen of source patient is known => prescribe 2 NRTIs and 1 protease inhibitor that are different from the source patient's regimen
- possible substitues for zidovudine and lamivudine:- stavudine (d4T/Zerit) 40mg bid for > 60kg and 30mg bid <> 60kg and 125mg for <>
Exposure to person or persons of unknown HIV status but who probably have high HIV risk factors :
- significant exposures => treat as if an exposure to a known HIV-infected person with an unknown medication regimen, as above
- exposures that might result in HIV infection => treat with zidovudine and lamivudine without a protease inhibitor
Exposure to person or persons of unknown HIV status but who probably have low HIV risk factors
- significant exposures => treat with zidovudine and lamivudine. A protease inhibitor could be added if the patient requests it, if the provider believes that the exposure history is unclear, other exposures also occurred, or if other factors relating to exposure history or HIV status are compelling
- exposures that might result in HIV infection => treat with zidovudine and lamivudine without a protease inhibitor
Additional caveats
* PEP should not be provided to patients whose exposure history has no known possibility for HIV transmission
* PEP should not be given to persons already infected with HIV
* providers may consider PEP for any patient who appears to be at risk after an HIV exposure but whose circumstances are not delineated in the above categories
Providers are reminded that PEP should only be prescribed as part of a comprehensive program to reduce future HIV risk-related behaviours. Multiple prescription requests for PEP should be strongly discouraged and must be averted through risk reduction counselling.
Definitions:
High HIV risk factors: trading sex for drugs or money, IV drug use, unprotected anal or vaginal intercourse with persons with HIV risk factors
Significant exposures include the following: anal or vaginal intercourse without a condom or with condom breakage; exposure to semen or blood onto mucosal or nonintact surfaces, and intravenous needle sharing
Examples of exposures that might result in HIV infection are as follows: cunnilingus, fellatio, semen or blood on healing skin wounds
TREATMENT OF Ramsay Hunt syndrome
*Medical:
.Corticosteroids and oral acyclovir are commonly used .Recently,combined therapy using corticosteroids plus intravenous acyclovir did not show benefit over corticosteroids alone in promoting facial nerve recovery after 6 months. However, randomized clinical trials evaluating both therapies are required.
.Vestibular suppressants may be helpful if vestibular symptoms are severe.
.As with Bell palsy, care must be taken to prevent corneal irritation and injury.
.Temporary relief of otalgia may be achieved by applying a local anesthetic or cocaine to the trigger point, if in the external auditory canal.
.Carbamazepine may be helpful, especially in cases of idiopathic geniculate neuralgia.
*Surgical:
Surgical decompression of the facial nerve has no role in this syndrome.
INVESTIGATION OF Ramsay Hunt Syndrome
Laboratory Studies:
1.The diagnosis of Ramsay Hunt syndrome is usually made without difficulty when the clinical characteristics are present. If necessary, varicella zoster virus (VZV) may be isolated from vesicle fluid and inoculated into susceptible human or monkey cells for identification by serologic means.
2.WBC count, erythrocyte sedimentation rate (ESR), and serum electrolytes are helpful in distinguishing the infectious and inflammatory nature of this syndrome.
3.As CNS complications are suspected (eg, meningitis, meningoencephalitis, myelitis, arteritis [large and small vessel], and ventriculitis), spinal fluid analysis and CNS imaging studies are recommended.
4.Viral studies ,
.VZV isolation in conventional cell culture is considered the definite diagnostic test. However, growing VZV in cell culture can be difficult and is usually too slow to be clinically helpful.
The sensitivity of conventional cell culture is 30-40%, with a specificity of 100%.
.Other tests, including Tzanck test, electron microscopy, and polymerase chain reaction (PCR) are generally more rapid and sensitive. The sensitivity of conventional PCR technique is estimated to be 60%.
.VZV has been detected by PCR in the tear fluid of patients with Bell palsy (prevalence, 25-35%).
.VZV antigen detection by direct immunofluorescence assay (DFA) is also possible, with sensitivity of 90% and specificity close to 99%.5
.Antibody determinations on paired sera may be helpful in establishing the diagnosis by comparing titers at time of presentation and a few weeks later.
Imaging studies:
-Structural lesions can be ruled out by CT scan, MRI, or magnetic resonance (MR) angiography.
-Gadolinium enhancement of the vestibular and facial nerves on MRI has been described in Ramsay Hunt syndrome.
-Recent advances in clinical MRI images (eg, 3-Tesla MRI, multichannel phased array coil, 3-dimensional fluid-attenuated inversion recovery [FLAIR]) allow the evaluation of subtle alterations at the level of the blood-labyrinthine barrier.
Tests:
-Audiometry usually reveals sensorineural hearing loss.
-Unilateral caloric weakness may be present on electronystagmography (ENG).
-Electrodiagnostic methods, such as facial motor nerve conductions studies (electroneurography), electromyography of facial innervated muscles, the blink reflex, and nerve excitability testing, could add information regarding the extent of seventh cranial nerve (CN VII) involvement, as well as prognostic factors.
Procedures:
-In the setting of a peripheral facial palsy, cerebrospinal fluid (CSF) rarely is analyzed. Although lumbar puncture is not recommended in the diagnosis of this disease, CSF findings can be helpful in confirming the diagnosis. In one study, CSF findings were abnormal in 11% of 239 patients with idiopathic peripheral facial palsy, in 60% of 17 patients with Ramsay Hunt syndrome (abnormal finding was pleocytosis), in 25% of 8 patients with Lyme disease, and in all 8 patients with HIV infection. Thus, if the CSF is abnormal, a specific cause should be sought.
-Temporary relief of otalgia in geniculate neuralgia may be achieved by applying a local anesthetic or cocaine to the trigger point, if in the external auditory canal.
Histologic Findings:
-The affected ganglia of the cranial nerve roots are swollen and inflamed.
-The inflammatory reaction is chiefly of a lymphocytic nature, but a few polymorphonuclear leukocytes or plasma cells may also be present.
-Some of the cells of the ganglia are swollen and others degenerated.
1.The diagnosis of Ramsay Hunt syndrome is usually made without difficulty when the clinical characteristics are present. If necessary, varicella zoster virus (VZV) may be isolated from vesicle fluid and inoculated into susceptible human or monkey cells for identification by serologic means.
2.WBC count, erythrocyte sedimentation rate (ESR), and serum electrolytes are helpful in distinguishing the infectious and inflammatory nature of this syndrome.
3.As CNS complications are suspected (eg, meningitis, meningoencephalitis, myelitis, arteritis [large and small vessel], and ventriculitis), spinal fluid analysis and CNS imaging studies are recommended.
4.Viral studies ,
.VZV isolation in conventional cell culture is considered the definite diagnostic test. However, growing VZV in cell culture can be difficult and is usually too slow to be clinically helpful.
The sensitivity of conventional cell culture is 30-40%, with a specificity of 100%.
.Other tests, including Tzanck test, electron microscopy, and polymerase chain reaction (PCR) are generally more rapid and sensitive. The sensitivity of conventional PCR technique is estimated to be 60%.
.VZV has been detected by PCR in the tear fluid of patients with Bell palsy (prevalence, 25-35%).
.VZV antigen detection by direct immunofluorescence assay (DFA) is also possible, with sensitivity of 90% and specificity close to 99%.5
.Antibody determinations on paired sera may be helpful in establishing the diagnosis by comparing titers at time of presentation and a few weeks later.
Imaging studies:
-Structural lesions can be ruled out by CT scan, MRI, or magnetic resonance (MR) angiography.
-Gadolinium enhancement of the vestibular and facial nerves on MRI has been described in Ramsay Hunt syndrome.
-Recent advances in clinical MRI images (eg, 3-Tesla MRI, multichannel phased array coil, 3-dimensional fluid-attenuated inversion recovery [FLAIR]) allow the evaluation of subtle alterations at the level of the blood-labyrinthine barrier.
Tests:
-Audiometry usually reveals sensorineural hearing loss.
-Unilateral caloric weakness may be present on electronystagmography (ENG).
-Electrodiagnostic methods, such as facial motor nerve conductions studies (electroneurography), electromyography of facial innervated muscles, the blink reflex, and nerve excitability testing, could add information regarding the extent of seventh cranial nerve (CN VII) involvement, as well as prognostic factors.
Procedures:
-In the setting of a peripheral facial palsy, cerebrospinal fluid (CSF) rarely is analyzed. Although lumbar puncture is not recommended in the diagnosis of this disease, CSF findings can be helpful in confirming the diagnosis. In one study, CSF findings were abnormal in 11% of 239 patients with idiopathic peripheral facial palsy, in 60% of 17 patients with Ramsay Hunt syndrome (abnormal finding was pleocytosis), in 25% of 8 patients with Lyme disease, and in all 8 patients with HIV infection. Thus, if the CSF is abnormal, a specific cause should be sought.
-Temporary relief of otalgia in geniculate neuralgia may be achieved by applying a local anesthetic or cocaine to the trigger point, if in the external auditory canal.
Histologic Findings:
-The affected ganglia of the cranial nerve roots are swollen and inflamed.
-The inflammatory reaction is chiefly of a lymphocytic nature, but a few polymorphonuclear leukocytes or plasma cells may also be present.
-Some of the cells of the ganglia are swollen and others degenerated.
Subscribe to:
Posts (Atom)
Popular Posts
-
W ind --- pneumonia, atelectasis at 1st 24- 48 hours W ater --- urinary tract infection at Anytime after post op day 3 W ound --- wound ...
-
Raccoon Eyes. Ecchymosis in the periorbital area, resulting from bleeding from a fracture site in the anterior portion of the skull base. Th...
-
Lymph Nodes : The major lymph node groups are located along the anterior and posterior aspects of the neck and on the underside of the jaw. ...
-
Fournier's gangrene is a rare condition and delayed treatment results in fatal outcome. We managed a case of Fournier's gangrene by...
-
Viewed posteriorly the right kidney has its upper edge opposite the 11th dorsal spine and the lower edge of the 11th rib. Its lower edge is ...
-
If you are palpating a swelling like an abdominal swelling infront of the aorta, You have to decide whether the mass you feel is pulsatile/e...
-
This raised skin lesion with a central necrotic area has the appearances of a keratoacanthoma. The natural history of these lesions is that...
-
The sphenoid bone carries its share of creating part of the base of the cranium. While it can be seen laterally and inferiorly, the shape of...