作者: Kristine M. Cornejo , Christopher A. Lum , Allan K. Izumi
DOI: 10.1097/DAD.0B013E31826FF6A6
关键词: Granuloma annulare 、 Myelodysplastic syndromes 、 Lymphoma 、 Interstitial granulomatous dermatitis 、 Pathology 、 Leukemia 、 Medicine 、 Leukemic Infiltration 、 Immunoglobulin D 、 Bone marrow
摘要: Cutaneous manifestations associated with myelodysplastic syndromes (MDS) are uncommon and can occur as specific or nonspecific lesions. Recognizing these cutaneous is important they precede blood bone marrow transformation to leukemia. Granulomatous reactions have rarely been described lesions of MDS. These rare cases histologically resembled granuloma annulare, sarcoid, a generalized dermal interstitial granulomatous dermatitis (IGD) which were not leukemic infiltration. The authors report an interesting case IGD-like eruption evolving over the course MDS eventual progression systemic IGD inflammatory reaction that refers varied spectrum histologic patterns variety illnesses hypersensitivity reactions, including lymphoma In patients MDS, surveillance for leukemia critical component their follow-up care. Normally, this occurs through serial peripheral smears studies. eruptions pattern may serve additional clinical indicator in Although primarily reactive pattern, entity harbor blasts.