Reticulohistiocytose multicentrique : a propos de deux observations

Introduction :La Reticulohistiocytose Multicentrique (RHM) est une affection peu decrite dans la litterature. Nous rapportons deux observations de RHM faites a Dakar; caracteristiques par l'agressivite des lesions et la presentation cutanee pure dans un cas.Observations : La premiere observation concernait une patiente agee de 34 ans admise pour des papulo nodules dissemines; une polyarthrite bilaterale asymetrique destructrice n'epargnant pas les inter-phalangiennes distales et un epanchement sero-hematique aux genoux. La deuxieme observation etait faite chez une patiente agee de 26 ans qui avait des papulo-nodules dissemines depuis 10 ans. L'examen histologique en faveur de la RHM dans les deux cas; montrait une infiltration intradermique d'histiocytes multinucleees sans plasmocytes ni polynucleaires ni cellules xanthomisees. La corticotherapie etait decevante dans la premiere observation. La surveillance etait indiquee dans le deuxieme cas. Conlusion : La RHM est une maladie rare chronique handicapante a localisation tegumentaire diffuse isolee exceptionnelle en Afrique

[Cutaneous leishmaniasis in hospital area: epidemiological and clinical aspects, about 16 cases]. / Leishmaniose cutanée en milieu hospitalier: aspects epidémiologiques et cliniques a propos de 16 observations.

Cutaneous leishmaniasis, a chronic infectious ulcerative skin disease caused by a protozoan parasite of the genus Leishmania, is transmitted by the bite of sandflies. We report 16 cases of cutaneous leishmaniasis observed in Dakar from 1990 to 2000. The aim of this retrospective study was to determine the epidemiological and clinical features. Their age range was 10 to 78 years (mean 41.12 years). The sex ratio was 3. The most commun presentation was the ulcero-crusted lesions (bouton d'orient) observed in 56.25% of cases. The other clinical presentation are the sporotrichoid lesions (25%), the lupoid lesions observed in 12.5% and the cutaneous diffus leishmaniasis in 12.5%. In all these cases, there were many lesions. On treatment we observed 87.5% of total remission.

[Squamous cell carcinoma in black patients: 80 cases]. / Carcinome épidermoïde sur peau noire: 80 cas.

INTRODUCTION: Squamous cell carcinoma is a malignant epithelial tumor of the skin, rarely observed in "black" skin. It often complicates an acquired or congenital pre-neoplastic dermatosis. We report on 80 cases of squamous cell carcinoma having occurred in black African patients from Senegal. PATIENTS AND METHODS: We retrospectively analyzed all the medical files of patients followed-up in the department for histologically confirmed squamous cell carcinoma from 1980 to 1999. RESULTS: Eighty cases of carcinoma were collected. The mean age of the patients was of 47 years (range: 1 to 85) and the sex ratio was of 1.35 (46 men and 34 women). A pre-neoplastic dermatosis was identified in 65% the patients. Acquired pre-neoplastic dermatosis was: heat burn scars (15 cases), chronic discoid lupus erythematosus (6 cases) and chronic phagedenic ulcer (4 cases). Pre-neoplastic genodermatoses were: albinism (6 cases), xeroderma pigmentosum (5 cases) and epidermodysplasia verruciformis (1 case). Lesions were multiple and cephalic in patients with genodermatosis. Death due to carcinoma occurred in 8 patients. COMMENTS: This large series of squamous cell carcinoma emphasizes: the rarity of squamous cell carcinomas in black patients and the frequency of its occurrence on acquired pre-existing dermatosis. For many years phagedenic ulcers predominated. Our results show the regression of the latter and its increase on post-burn scars and chronic lupus erythematosus. Pre-neoplastic genodermatoses that determine multiple cancers, usually located on sun-exposed areas and occurring in young patients, are particularly severe.

[Systemic scleroderma: 92 cases in Dakar]. / La sclérodermie systémique à Dakar: à propos d'une série de 92 cas.

We performed a retrospective study in order to characterize epidemiological data and signs of systemic scleroderma in Sénégal. All patients with the diagnosis according the ACR's criteria of scleroderma were recruited. We included 92 patients, the mean age was 33 years and sex ratio male to female was 0.19 (15 men and 77 women). There were 8 children in our series (8.9%). The initial complaints were cutaneous manifestations (64%) and Raynaud's syndrome (16.3%). Clinical manifestations at admission were muco-cutaneous (100%), osteo-articular and muscular (59%) and Raynaud's syndrome (57%). Focal hypopigmentation was common (70%). Anti-nuclear antibodies were present in 67.4% of patients. Skin biopsy was contributive in all patients in which it was performed (79 cases). Electrocardiogram was abnormal in 55%, non specific inflammatory syndrome was present in 44% and pulmonary function was abnormal in 52%. Our data suggest that systemic scleroderma is more common in younger people in black population. Disorders of pigmentation are common and Raynaud's syndrome is uncommon.