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原发性腰肌间叶性原始神经外胚层肿瘤:一例报告及文献复习。

Primary anaplastic large cell lymphoma of the psoas muscle: a case report and literature review.

机构信息

Department of Pediatrics, Wakayama Medical University, Wakayama City, Japan.

出版信息

Acta Haematol. 2012;127(3):186-8. doi: 10.1159/000335744. Epub 2012 Feb 18.

Abstract

Primary anaplastic large cell lymphoma (ALCL) of skeletal muscle is very rare. We report a case of ALCL arising from the left psoas muscle. A 14-year-old girl presented with a large left inguinal tumor. She complained of a 2-month history of left leg pain, which had been exacerbated upon leg extension, and she had become aware of a rapidly growing left inguinal tumor 3 weeks before admission. CT scan and MRI revealed a large tumor arising from the left major psoas muscle and protruding into the inguinal region. In view of the tumor's location and the patient's age, soft tissue tumors such as rhabdomyosarcoma and primitive neuroectodermal tumor were initially considered. However, histopathological examination yielded a diagnosis of anaplastic lymphoma kinase-positive ALCL. The serum level of soluble interleukin-2 receptor was markedly elevated at 50,414 U/ml, and this also strongly suggested ALCL. Although rarely reported, ALCL is an important entity to consider in the differential diagnosis of skeletal muscle tumors in children and young adults.

摘要

原发性间变性大细胞淋巴瘤(ALCL)非常罕见。我们报告了一例发生于左腰肌的 ALCL。一名 14 岁女孩因左侧巨大腹股沟肿瘤就诊。她诉左腿疼痛 2 个月,在伸展腿部时加剧,并在入院前 3 周发现左侧腹股沟肿瘤迅速增大。CT 扫描和 MRI 显示一个源自左大腰肌并向腹股沟区域突出的大型肿瘤。鉴于肿瘤的位置和患者的年龄,最初考虑了横纹肌肉瘤和原始神经外胚层肿瘤等软组织肿瘤。然而,组织病理学检查诊断为间变性淋巴瘤激酶阳性 ALCL。血清可溶性白细胞介素 2 受体水平显著升高,达到 50414 U/ml,这也强烈提示为 ALCL。尽管罕见报道,但 ALCL 是儿童和年轻成人骨骼肌肿瘤鉴别诊断中需要考虑的重要实体。

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