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膀胱间变性淋巴瘤激酶1阳性炎性肌成纤维细胞瘤:一种具有诊断和治疗意义的罕见间叶性肿瘤

Anaplastic lymphoma kinase1 positive inflammatory myofibroblastic tumor of the urinary bladder: A rare mesenchymal neoplasm with diagnostic and therapeutic implications.

作者信息

Poombal Fnu, Mansoor Ibrahim, Abdellatif Randa M, Shaker Nada

机构信息

Department of Pathology, UMass Chan Medical School - Baystate Regional Campus Ringgold standard institution, Springfield, MA, USA.

Department of Pathology, Kings College London, Jeddah, Saudi Arabia.

出版信息

SAGE Open Med Case Rep. 2024 Dec 19;12:2050313X241308992. doi: 10.1177/2050313X241308992. eCollection 2024.

Abstract

Inflammatory myofibroblastic tumors (IMTs) are rare mesenchymal neoplasms characterized by spindle-cell morphology with accompanying inflammatory infiltrates. Originally described in 1939, these tumors can arise in various anatomic locations, with the urinary bladder being a rare site of occurrence but the most common within the genitourinary tract. IMTs typically present as polypoid masses or firm submucosal nodules, often with painless hematuria in bladder cases. Histopathologically, IMTs are composed of myofibroblasts with myxoid stroma and mixed inflammatory cells, predominantly lymphocytes and plasma cells. Immunohistochemically, these tumors commonly express anaplastic lymphoma kinase1 (ALK1), vimentin, smooth muscle actin (SMA), and cytokeratin, with ALK1 serving as a crucial marker for diagnosis. This report details the case of a 31-year-old female presenting with hematuria, found to have a soft tissue mass in the urinary bladder (5.0 × 3.0 cm). Imaging revealed a well-defined lesion with vascularity. Histopathological examination confirmed an IMT, with immunohistochemistry showing diffuse ALK1 positivity, patchy SMA staining, and variable desmin expression, consistent with the diagnosis. IMTs are generally considered neoplasms of intermediate malignant potential. While metastasis is exceedingly rare in bladder IMTs, local recurrence has been reported, particularly in cases of incomplete surgical resection. Recent advances highlight the role of ALK inhibitors in managing unresectable cases, enabling partial cystectomy in select patients. This article underscores the importance of achieving complete surgical excision and highlights the role of ALK expression in diagnosis and differentiation from other spindle-cell neoplasms. Further studies are needed to elucidate the molecular and clinical factors influencing prognosis and to refine treatment strategies for IMTs.

摘要

炎性肌纤维母细胞瘤(IMTs)是一种罕见的间叶性肿瘤,其特征为梭形细胞形态并伴有炎性浸润。这些肿瘤最初于1939年被描述,可发生于各种解剖部位,膀胱是罕见的发生部位,但却是泌尿生殖道中最常见的部位。IMTs通常表现为息肉样肿块或坚实的黏膜下结节,膀胱病例中常伴有无痛性血尿。组织病理学上,IMTs由肌成纤维细胞、黏液样基质和混合性炎性细胞组成,主要为淋巴细胞和浆细胞。免疫组织化学方面,这些肿瘤通常表达间变性淋巴瘤激酶1(ALK1)、波形蛋白、平滑肌肌动蛋白(SMA)和细胞角蛋白,ALK1是诊断的关键标志物。本报告详细介绍了一名31岁女性因血尿就诊的病例,发现膀胱有一个软组织肿块(5.0×3.0 cm)。影像学检查显示病变边界清晰且有血管。组织病理学检查确诊为IMT,免疫组织化学显示ALK1弥漫阳性、SMA呈斑片状染色以及结蛋白表达各异,与诊断相符。IMTs一般被认为是具有中等恶性潜能的肿瘤。虽然膀胱IMTs转移极为罕见,但有局部复发的报道,尤其是在手术切除不完全的病例中。最近的进展突出了ALK抑制剂在处理不可切除病例中的作用,使部分患者能够接受部分膀胱切除术。本文强调了实现完整手术切除的重要性,并突出了ALK表达在诊断以及与其他梭形细胞肿瘤鉴别中的作用。需要进一步研究以阐明影响预后的分子和临床因素,并完善IMTs的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f2/11660058/451e232f4ea1/10.1177_2050313X241308992-fig1.jpg

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