Gafter U, Kessler E, Shabtay F, Shaked P, Djaldetti M
J Clin Pathol. 1980 Feb;33(2):136-44. doi: 10.1136/jcp.33.2.136.
A patient with alpha heavy chain disease (alphaHCD), who showed an abnormal chromosomal marker (D14 q+) in 10% of the bone marrow cells, is described. The mesenteric lymph nodes, which showed reactive hyperplasia in the first biopsy, transformed later to a malignant lymphoma and finally to a plasma cell tumour. The small intestine revealed villous atrophy, diminished crypts, and intact surface epithelium. The ultrastructure of the goblet and epithelial cells appeared to be normal, and the microvilli were preserved except for circumscribed areas of destruction. The lamina propria was heavily infiltrated with mononuclear cells, mainly mature plasma cells. Alpha heavy chains (alphaHC) were found in the patient's saliva.
本文描述了一名患有α重链病(alphaHCD)的患者,其10%的骨髓细胞显示出异常染色体标记(D14 q+)。肠系膜淋巴结在首次活检时表现为反应性增生,随后转变为恶性淋巴瘤,最终发展为浆细胞瘤。小肠显示绒毛萎缩、隐窝减少,表面上皮完整。杯状细胞和上皮细胞的超微结构似乎正常,微绒毛除了有局限性破坏区域外均得以保留。固有层有大量单核细胞浸润,主要是成熟浆细胞。在患者的唾液中发现了α重链(alphaHC)。