Uthamalingam Preithy, Mehta Sangita
1 Kovai Medical Center and Hospital, Coimbatore, Tamil Nadu, India.
Int J Surg Pathol. 2017 Aug;25(5):458-461. doi: 10.1177/1066896917696746. Epub 2017 Feb 1.
Crystal-storing histiocytosis (CSH) is a rare histiocytic lesion, most often described in association with lymphoid malignancies, especially plasma cell myeloma or lymphomas associated with monoclonal gammopathy. A few cases have also been described in patients without an underlying lymphoid/plasmacytic neoplasm. The histiocytes are characterized by intralysosomal accumulation of crystals composed of whole or part of the immunoglobulin molecule. The pathobiology is largely unclear. It is a rare phenomenon and the available literature is restricted to case reports and a few case series. We present a case of a 70-year-old gentleman who presented with pathological fracture of left neck of femur secondary to CSH, a presentation so far unreported in the literature. Because of associated clinical features, a plasma cell dyscrasia was suspected and the workup, including bone marrow biopsy, yielded a diagnosis of plasma cell myeloma. Histological examination of the excised femoral head showed near complete replacement of the marrow spaces with sheets of histocytes rich in intracytoplasmic crystals and only occasional plasma cells. The peculiar presentation with pathological fracture of femur in the index case and predominant tumefactive lesions in the cases in the literature might suggest a possible neoplastic origin of this lesion.
晶体贮积性组织细胞增多症(CSH)是一种罕见的组织细胞病变,最常被描述为与淋巴系统恶性肿瘤相关,尤其是与单克隆丙种球蛋白病相关的浆细胞骨髓瘤或淋巴瘤。也有少数病例在无潜在淋巴样/浆细胞性肿瘤的患者中被描述。组织细胞的特征是溶酶体内积累由全部或部分免疫球蛋白分子组成的晶体。其病理生物学在很大程度上尚不清楚。这是一种罕见现象,现有文献仅限于病例报告和少数病例系列。我们报告一例70岁男性患者,因CSH继发左股骨颈病理性骨折,这种表现迄今未见文献报道。由于相关的临床特征,怀疑存在浆细胞异常增生,经包括骨髓活检在内的检查,诊断为浆细胞骨髓瘤。对切除的股骨头进行组织学检查显示,骨髓腔几乎完全被富含胞质内晶体的组织细胞片层取代,仅偶尔可见浆细胞。该病例中股骨病理性骨折的特殊表现以及文献中病例的主要肿胀性病变可能提示该病变可能起源于肿瘤。