Walker P D, Rosai J, Dorfman R F
Am J Clin Pathol. 1981 Feb;75(2):131-9. doi: 10.1093/ajcp/75.2.131.
The cases of five patients who had sinus histiocytosis with massive lymphadenopathy accompanied by osseous involvement by the disease are presented. Four of the five patients were children. The bone lesions were multiple in four cases and solitary in one. The long bones were most commonly involved (three patients); other bones affected were the skull, vertebral bodies, pelvis, phalanges, metacarpals, and ribs. Roentgenograms showed lytic lesions with ill-defined, non-sclerotic margins. Microscopically, the lesions consisted of an inflammatory infiltrate composed primarily of mature histiocytes (sometimes demonstrating lymphocytophagocytosis) and accompanied by plasma cells and lymphocytes. The roentgenographic differential diagnosis includes histiocytosis X, metastatic malignancy, sarcoidosis, storage disorders, and the bone lesions of neurofibromatosis.
本文报告了5例伴有骨受累的窦性组织细胞增多症伴巨大淋巴结病患者的病例。5例患者中有4例为儿童。4例患者的骨病变为多发,1例为单发。长骨最常受累(3例患者);其他受累骨骼包括颅骨、椎体、骨盆、指骨、掌骨和肋骨。X线片显示溶骨性病变,边界不清,无硬化边缘。显微镜下,病变由主要由成熟组织细胞组成的炎性浸润(有时显示淋巴细胞吞噬现象)组成,并伴有浆细胞和淋巴细胞。X线鉴别诊断包括组织细胞增多症X、转移性恶性肿瘤、结节病、贮积病和神经纤维瘤病的骨病变。