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Last Updated: May 12th, 2008 - 03:38:23 |
Title: Disseminated Papules
Presenter: Igor Chaplik, D.O., Charles Gropper, M.D., Cindy Hoffman, D.O.
Dermatology Program: St. Barnabas Hospital Dermatology Department, Bronx, New York
Program Director: Cindy Hoffman, D.O.
Submitted on:
Aug 31, 2003
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CHIEF COMPLAINT:
Fever, cough, intermittent headaches, weakness, shortness of breath, and a twenty-pound weight loss over the last month.
CLINICAL HISTORY:
Signs and symptoms:
Previous Treatment:
Other information:
PHYSICAL EXAM:
The physical exam revealed a cachectic, febrile patient with a temperature of 102.4 F. He was breathing rapidly at 18 breaths per minute, and his heart rate was 76. His blood pressure was 90/66. His skin exam revealed several, discrete, dome-shaped, some umbilicated, papules on the abdomen and chest. Also present were several, hyperpigmented, scaly plaques on his abdomen and chest. (Fig. 1 and 2). Bilateral inguinal and axillary lymph nodes were palpable. Auscultation of the lungs revealed bilateral rales and rhonchi.
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| Fig. 1 showing numerous, discrete, dome-shaped, some umbilicated papules and several, fairly well-defined, hyperpigmented, scaly plaques on abdomen and chest |
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| Fig. 2 Close-up of umbilicated papule |
LABORATORY TESTS:
The patient’s complete blood count revealed a white count of 8600, with 84.9% neutrophils. His hemoglobin was low at 10.2 g/dl and his hematocrit low at 31.1%. The patient was found to be HIV positive, with a CD4<20 cells microliter and an rna by pcr of 69965 copies ml/
DERMATOHISTOPATHOLOGY:
His skin biopsy revealed numerous organisms of various sizes surrounded by capsules, which stained positive with mucicarmine in the superficial and deep dermis, with very little inflammatory response. (Fig 3,4)
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| Fig3. H & E stain of 3mm punch biopsy at 10X showing numerous encapsulated organisms in the superficial and deep dermis with very little inflammatory response |
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| Fig. 4. Mucicarmine stain of 3mm punch biopsy at 40X showing the characteristic red staining capsule in the superficial dermis |
DIFFERENTIAL DIAGNOSIS:
1. Coccidioides imitis
2. Penicillium marneffei
3. Cryptococcus neoformans
4. Histoplasma capsulatum
5. Tuberculosis
SCROLL DOWN FOR ANSWER AND DISCUSSION.
CORRECT DIAGNOSIS:
Cryptococcus neoformans
DISCUSSION:
Cryptococcus neoformans is an encapsulated yeast like fungus. Strains are grouped into two varieties that include five serotypes known as C. neoformans variety neoformans (serotypes A, D, and AD) and C. neoformans variety gattii (serotypes B and C). The serotype differences reflect antigenic differences in the structure of the capsular polysaccharide. C. neoformans var. neoformans is found throughout the world in association with excreta from certain birds including pigeons, chickens, canaries, and cockatoos. C. neoformans var. gattii is found primarily in tropical and subtropical regions and has been associated with several species of eucalyptus trees.
In order to cause disease in humans, the fungus must be inhaled into the lungs, although a small percentage of patients can develop primary cutaneous cryptococcus after direct implantation. Once within the lungs, C. neoformans can cause a variety of symptoms from asymtomatic colonization to severe pneumonia. From the lungs, the organisms disseminate to the blood and subsequently any organ system. The CNS is the most common site of dissemination.
The skin is the second most common site of cryptococcal dissemination, occurs in 10-20% of patients, and is often the presenting sign of disease. Cutaneous manifestations of disseminated disease are protean and most commonly occur on the head and neck. Although molluscum-like lesions are the most common, acneiform lesions, purpura, vesicles, tumors, abscesses, oral and genital ulcers, granulomas, plaques, sinus tracts, cellulitis, subcutaenous nodules, and HSV-like lesions have all been reported. Direct cutaneous cryptococcosis caused by direct trauma is rare and produces solitary nodules that ultimately break down or ulcerate. Lymphadenopathy may or not be present. Biopsy specimens will often show two types of histological patterns: gelatinous and granulomatous. This patient’s biopsy consisted of the gelatinous type, which produces little inflammatory reaction and numerous organisms (4 to 12 mum) with large polysaccharide capsules. The capsule stains purple with methylene blue, blue with alcian blue, and red with mucicarmine. The granulomatous type produces more of an inflammatory reaction with giant cells and a small number of organisms. The organisms are 2 to 4 mum, have thin or no capsules, and are found within giant or mononuclear cells. The fungi stain red with PAS, black with methanamine silver, and dark brown with Fontana-Masson.
TREATMENT:
Once disseminated cryptococcosis has been ascertained, the treatment approach relies heavily on amphotericin B (0.7-1 mg/kg/d) plus flucytosine (100 mg/kg/d for 2 weeks) followed by fluconazole (400 mg/d) for a minimum of 10 weeks in the immunocompromised host. Amphotericin was used to treat this patient.
Other Treatment options:
Ambisone at 4 mg/kg/day has been shown to perform similar to Amphotericin B. Fluconazole (400-800 mg/d) plus flucytosine (100-150 mg/kg/ d) for 6 weeks is an alternative to the use of amphotericin B, although toxicity with this regimen is high. For those patients with HIV who present with isolated pulmonary or urinary tract disease, fluconazole (200-400 mg/d) is indicated and itraconazole (200-400 mg/d) is an acceptable alternative.
REFERENCES:
1. Schupbach DW, Wheeler CE, Briggaman RA, et al.Cutaneous manifestations of disseminated Cryptococcus. Arch Dermatol 1976;112:1734-40.
2. Perfect JR. Cryptococcosis. Infect Dis Clin North Am 1989;3:77-102.
3. Dimino-Emme L. Cutaneous manifestations of disseminated Cryptococcus. J Am Acad Dermatol 1995; 32(5 Pt 2): 844-50
4. Bennett JE, Dismukes W, Duma RJ, Medoff G, Sande MA, Gallis H, et al. A comparison of amphotericin B alone and combined with flucytosine in the treatment of cryptococcal meningitis. N Engl J Med 1979;301:126-31
5. Lever WF, Schaumberg-Lever G. Histopathology of the skin. Philadelphia: JB Lippincott, 1990:379-81
Additional Comment:
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