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This article discusses a case of a 16-year-old boy who presented with a pustular rash on his back. The rash was large and formed annular crusted lesions with a pustular border. The boy did not have any associated symptoms and his general health was good. After conducting various tests and a skin biopsy, the diagnosis was determined to be subcorneal pustular dermatosis (SCPD), a rare neutrophilic dermatosis. The boy was treated with topical steroid and oral dapsone, which led to complete remission. SCPD is typically seen in middle-aged or elderly women, making it rare in children and adolescents. The differential diagnosis includes other skin conditions such as pustular psoriasis and autoimmune bullous dermatoses. It is important to rule out associated systemic diseases, as SCPD can be associated with various conditions. The first-line treatment for SCPD is dapsone, but other treatments may be used if dapsone is ineffective or contraindicated. SCPD, although rare in childhood, should be considered as a possible cause of pustular eruptions in children. [Extracted from the article]

Background Few studies have been published on the histopathology of cutaneous adverse drug reactions ( CADR), and most of these lack information on skin allergological tests. The histopathology of drug reaction with eosinophilia and systemic symptoms ( DRESS) is also seldom described. The purpose of our study was to examine six types of well-documented CADR (maculopapular exanthema, DRESS, fixed drug eruption, Stevens-Johnson syndrome, toxic epidermal necrolysis [ TEN], and acute generalized exanthematous pustulosis) using histopathology and immunohistochemistry to evaluate the expression of granulysin, a key molecule in TEN. Methods We retrospectively included 106 skin biopsies performed in proven cases of CADR (by chronological investigation, single attributable drug, or/and skin tests). All slides were reviewed, and microscopic changes were analyzed using a standardized form. Granulysin expression was studied by immunohistochemistry. Results In DRESS, we observed spongiosis, edema, and basal vacuolization, with rare necrotic keratinocytes and constant lymphocytic infiltrate in the superficial dermis. Eosinophils were often present, and pustules were found in 15% of cases. Necrotic keratinocytes are often absent in maculopapular exanthema. Granulysin was expressed in six types of CADR with a trend toward more intense expression in DRESS and TEN. Conclusion We detailed further about the histopathology of DRESS. Granulysin expression was observed in all CADR with a marked overlap of expression pattern between the six types. [ABSTRACT FROM AUTHOR]

Oseltamivir is a neuraminidase inhibitor approved for the prevention and treatment of influenza. Few haematological side effects have been reported with oseltamivir. We report herein the case of an unexpected platelet increase in a 46-year-old woman with idiopathic thrombocytopenia ( ITP) treated with oseltamivir for influenza. The mechanism may involve the neuraminidase inhibition which decrease platelet surface sialic acid content and reduce their removal by the reticuloendothelial system. Oseltamivir may be responsible for platelet increase especially in patients with ITP. [ABSTRACT FROM AUTHOR]