hiv阴性儿童胫骨浆母细胞淋巴瘤:一种新的口外定位。

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2022-06-08 eCollection Date: 2022-01-01 DOI:10.1155/2022/4353830
Ali Mala, Yameena Noman Khan, Akbar Ahmed, Naema Khayyam, Kanwal Aftab
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引用次数: 1

摘要

浆母细胞淋巴瘤是一种侵袭性高级别非霍奇金淋巴瘤,主要见于hiv感染者。除了与HIV有很强的相关性外,PBL还可以在免疫功能低下的HIV阴性患者中表现出来。巴基斯坦卡拉奇的印度河医院和健康网络(IHHN)报道了一名免疫功能正常且其他方面健康的儿童患PBL的罕见病例。患者有右腿肿胀和疼痛的主诉,从信德省一个城市转诊过来。组织病理学分析显示肿瘤片和聚集体取代骨髓,穿插硬化骨碎片。大的,单形的,多核的肿瘤细胞含有丰富的细胞质和分散的多形性细胞,也被注意到,导致胫骨浆母细胞淋巴瘤的诊断。采用FAB/LMB96 C组化疗方案治疗侵袭性和高危癌症,临床症状明显改善。
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Tibial Plasmablastic Lymphoma in a HIV-Negative Child: A Novel Extraoral Localisation.

Plasmablastic lymphoma is an aggressive, high-grade non-Hodgkin lymphoma predominantly seen in HIV-infected individuals. Alongside a strong correlation with HIV, PBL can manifest in immunocompromised HIV-negative patients. A rare case of PBL in an immunocompetent and otherwise healthy child presented to Indus Hospital & Health Network (IHHN), Karachi, Pakistan. The patient had complaints of swelling and pain in the right leg and was referred from a city in Interior Sindh. Histopathological analysis revealed sheets and aggregates of neoplasm replacing bone marrow interspersed with sclerotic bony fragments. Large, monomorphic, multinucleated neoplastic cells containing abundant cytoplasm and scattered pleomorphic cells were also noted, leading to the diagnosis of tibial plasmablastic lymphoma. A FAB/LMB96 group C chemotherapy regimen for aggressive and high-risk cancer was administered with a marked improvement in clinical symptoms.

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审稿时长
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