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1.
Indian J Dermatol Venereol Leprol ; 2016 Mar-Apr; 82(2): 239
Article in English | IMSEAR | ID: sea-178189
2.
Indian J Dermatol Venereol Leprol ; 2015 Mar-Apr; 81(2): 170-173
Article in English | IMSEAR | ID: sea-158275

ABSTRACT

Merkel cell carcinoma is an aggressive and frequently lethal tumor of the elderly, associated with sun exposure and immunosuppression which is less common in the dark-skinned. We report the case of a 40-year-old woman who presented with multiple slowly progressive, mildly itchy ulcerated plaques of size ranging from 2 × 3 cm to 5 × 7 cm on the left knee of 1 year duration. Skin biopsy showed diffuse dermal infi ltration by small round cells with molding of cells and lymphocyte infi ltration. The cells stained positive for cytokeratin (CK) 20, CK7, neuron-specifi c enolase, and chromogranin. The skin lesions underwent spontaneous regression within 1 month of skin biopsy and have not recurred during the past 2 years. The immune mechanisms triggered by biopsy possibly explain the spontaneous regression.


Subject(s)
Adult , Female , Humans , Keratin-7 , Remission, Spontaneous/immunology
3.
Indian J Dermatol Venereol Leprol ; 2009 Sept-Oct; 75(5): 517-518
Article in English | IMSEAR | ID: sea-140434
4.
Indian J Dermatol Venereol Leprol ; 2005 Sep-Oct; 71(5): 325-8
Article in English | IMSEAR | ID: sea-52043

ABSTRACT

BACKGROUND: Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are a group of severe life threatening drug reactions. The drugs commonly implicated as the cause of these drug reactions vary depending on host factors and the prescription pattern of drugs in that particular area. AIM: The aim of the study was to find the drugs implicated as the cause of SJS/TEN in the patients admitted in the dermatology ward at the Medical College, Thrissur and to find the clinical outcome. METHODS: It was a retrospective study of 7 years from 1997 to 2004. The case records of all patients with a clinical diagnosis of TEN or SJS were studied in detail regarding the drugs implicated as the cause, the management and the clinical outcome. RESULTS: During the study period, 41 patients in the age group ranging from 12 to 72 years were treated as inpatients, of which 20 were males and 21 were females. The commonest drug implicated as the cause of SJS/TEN was carbamazepine (44%). The indication for carbamazepine was control of pain in more than 50% of the cases. Presence of a major systemic disease before the onset of SJS/TEN was associated with a bad prognosis. CONCLUSION: The increased use of carbamazepine, especially for control of pain, may be the reason for the increased incidence of SJS/TEN due to the same drug. Awareness about the drugs implicated in life threatening drug reactions will help physicians in preventing them by judicious use of the drugs.


Subject(s)
Adolescent , Adult , Aged , Amoxicillin/adverse effects , Anti-Bacterial Agents/adverse effects , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Anticonvulsants/adverse effects , Antipsychotic Agents/adverse effects , Carbamazepine/adverse effects , Child , Chlorpromazine/adverse effects , Stevens-Johnson Syndrome/etiology , Female , Humans , Male , Middle Aged , Retrospective Studies , Stevens-Johnson Syndrome/chemically induced
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