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Lambda-Restricted Crystal-Storing Histiocytosis of Stomach: A Case Report and Review of Literature

机译:Lambda限制晶体储存的胃组织植物症:一个案例报告和文学审查

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摘要

Crystal-storing histiocytosis (CSH) is a rare tissue phenomenon that is usually associated with lympho-proliferative diseases. The disease is characterized by prominent collections of macrophages with abundant eosinophilic cytoplasm and fibrillary cytoplasmic inclusions. The inclusions appear as linear crystals within the macrophages which are usually kappa restricted. The disease usually involves lungs, lymph nodes, bone marrow, thymus and spleen with rare involvement of the gastrointestinal tract. We report a rare case of lambda-restricted CSH of the stomach.?The diagnosis of CSH triggered further hematological evaluation. The patient was later diagnosed to have diffuse large B-cell lymphoma involving lymph nodes and bone marrow. He received?chemotherapy for the same and is on regular follow up. The index case highlights the need to identify CSH of stomach prompting evaluation for hematological malignancies and to increase its awareness among clinicians and pathologists.
机译:晶体储存的组织细胞症(CSH)是一种罕见的组织现象,通常与淋巴增殖性疾病相关。 该疾病的特征是突出的巨噬细胞收集,具有丰富的嗜酸性细胞质和纤维状细胞质夹杂物。 夹杂物在巨噬细胞内显示为直链晶体,这通常是κ受限制的。 该疾病通常涉及肺,淋巴结,骨髓,胸腺和脾脏,胃肠道罕见。 我们报告了一个罕见的胃肠局限性的胃部案例。CSH的诊断引发了进一步的血液学评估。 患者稍后被诊断为涉及淋巴结和骨髓的弥漫性大B细胞淋巴瘤。 他收到了?化学疗法同样的,正常随访。 索引案例突出了鉴定胃促使血液恶性恶性肿瘤的CSH的需要,并提高其在临床医生和病理学家之间的认识。

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