Keen C E, Philip G, Parker B C, Souhami R L
Department of Histopathology, Kingston Hospital, Surrey, UK.
Pathol Res Pract. 1990 Aug;186(4):519-25; discussion 526. doi: 10.1016/S0344-0338(11)80475-9.
We present an unusual case of multifocal Histiocytosis X in a 78-year-old man treated for Hodgkin's Disease 33 and 24 years previously. The Hodgkin's Disease at first involved cervical nodes and 9 years later axillary and inguinal nodes and was treated by radiotherapy. Chronic destructive lesions developed in the femora and pelvis and bone biopsies showed a curious mixture of fibroblastic tissue and foamy macrophages. These lesions eventually resulted in pathological fractures of the femoral necks, and bilateral hip replacements were required seven years after initial detection of the bony lesions. There was a focal infiltrate of S-100 protein positive histiocytic cells containing Birbeck granules in the femoral heads. There was radioisotopic and radiological evidence of other skeletal lesions. The association between Histiocytosis X and Hodgkin's Disease is recognised but rare and its significance is discussed.
我们报告了一例罕见的多灶性组织细胞增多症X病例,患者为一名78岁男性,曾在33年前和24年前接受过霍奇金淋巴瘤治疗。霍奇金淋巴瘤最初累及颈部淋巴结,9年后累及腋窝和腹股沟淋巴结,并接受了放射治疗。股骨和骨盆出现慢性破坏性病变,骨活检显示成纤维组织和泡沫巨噬细胞的奇特混合。这些病变最终导致股骨颈病理性骨折,在首次发现骨病变7年后需要进行双侧髋关节置换。股骨头有S-100蛋白阳性的组织细胞浸润,其中含有伯贝克颗粒。还有其他骨骼病变的放射性同位素和放射学证据。组织细胞增多症X与霍奇金淋巴瘤之间的关联已得到认可,但很罕见,本文将讨论其意义。