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色素性荨麻疹患者发生的血液系统恶性肿瘤。

Hematologic malignancies occurring in patients with urticaria pigmentosa.

作者信息

Cooper A J, Winkelmann R K, Wiltsie J C

出版信息

J Am Acad Dermatol. 1982 Aug;7(2):215-20. doi: 10.1016/s0190-9622(82)70110-0.

Abstract

Six patients had hematologic malignancies and coincident urticaria pigmentosa, five with the disseminated maculopapular form and one with the plaque form. Two patients had the juvenile-onset variety; the remainder had the adult eruptive variety. None of the patients complained of symptoms that could be attributed to liberation of histamine. In the two patients with juvenile-onset urticaria pigmentosa, the hematologic malignancies developed at the age of 17 years; one had Hodgkin's disease, and the other had acute myelomonocytic leukemia. In three patients with adult eruptive urticaria pigmentosa, the cutaneous lesions developed within 12 months of the diagnoses of lymphocytic lymphoma (two patients) and evolving myelomonocytic leukemia (one patient). In the remaining patient, cutaneous lesions developed many years before chronic lymphocytic leukemia was diagnosed. None of the patients had systemic mastocytosis. Skin biopsy specimens from all six patients showed an increase in dermal and perivascular round cells, and mast cells were seen in specimens from five of the six patients. In patients who received cytotoxic drugs for the hematologic malignancy, there was no change in the urticaria pigmentosa.

摘要

6例患者患有血液系统恶性肿瘤并伴有色素性荨麻疹,其中5例为播散性斑丘疹型,1例为斑块型。2例患者为青少年发病型,其余为成人发疹型。所有患者均未主诉可归因于组胺释放的症状。在2例青少年发病型色素性荨麻疹患者中,血液系统恶性肿瘤在17岁时发生;1例患有霍奇金病,另1例患有急性粒单核细胞白血病。在3例成人发疹型色素性荨麻疹患者中,皮肤损害在诊断淋巴细胞淋巴瘤(2例患者)和进展期粒单核细胞白血病(1例患者)后的12个月内出现。在其余患者中,皮肤损害在慢性淋巴细胞白血病诊断多年前就已出现。所有6例患者均无系统性肥大细胞增多症。所有6例患者的皮肤活检标本均显示真皮和血管周围圆形细胞增多,6例患者中有5例的标本中可见肥大细胞。接受细胞毒性药物治疗血液系统恶性肿瘤的患者,色素性荨麻疹无变化。

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