Willis S M, Opal S M, Fitzpatrick J E
Arch Dermatol. 1985 Jul;121(7):910-3. doi: 10.1001/archderm.121.7.910.
Systemic histiocytosis was found in a patient who presented with chronic, nodular, and ulcerative skin lesions. The patient's hospital course was complicated by persistent fever, thrombocytopenia, severe neutropenia, and coagulation abnormalities. Treatment consisted only of splenectomy and supportive care. Postoperatively, the patient's skin lesions and the fever, pancytopenia, and coagulopathy resolved. Marked proliferation of histologically benign macrophages was observed in dermal, splenic, hepatic, and lymphoid tissues; leukophagocytosis and erythrophagocytosis were clearly demonstrated. This illness is most consistent with cytophagic histiocytic panniculitis, a newly described syndrome.
在一名出现慢性、结节性和溃疡性皮肤病变的患者中发现了系统性组织细胞增多症。该患者的住院过程因持续发热、血小板减少、严重中性粒细胞减少和凝血异常而变得复杂。治疗仅包括脾切除术和支持性护理。术后,患者的皮肤病变以及发热、全血细胞减少和凝血病均得到缓解。在皮肤、脾脏、肝脏和淋巴组织中观察到组织学上良性巨噬细胞的显著增殖;明显可见白细胞吞噬和红细胞吞噬现象。这种疾病与噬血细胞性组织细胞性脂膜炎最为相符,这是一种新描述的综合征。