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一名患有盲肠癌的患者的睾丸炎性肌纤维母细胞瘤。

Inflammatory Myofibroblastic Tumor of the Testis in a Patient With Cecal Carcinoma.

作者信息

Chandramouli R, Sowmya Y Sree, Raghava Ks Abhishek, Gochhait Debasis, Jagadesan Pandjatcharam

机构信息

Radiation Oncology, Krishna Cancer Institute, Cuddalore, IND.

Radiation Oncology, Great Eastern Medical School and Hospital, Ragolu, IND.

出版信息

Cureus. 2023 Sep 2;15(9):e44573. doi: 10.7759/cureus.44573. eCollection 2023 Sep.

Abstract

Inflammatory myofibroblastic tumors (IMTs) are uncommon tumors that can be classified among fibroinflammatory disorders. IMTs are diagnosed after excluding all other entities, which can be considered differential diagnoses of IMTs. Microscopic examination of IMTs shows multiple myofibroblastic spindle cells, which are surrounded by inflammation. IMTs have lesser chances of progression to malignancy. The case defined below is one of the few cases in the literature that reports the presentation of IMT and another malignancy. We describe a 72-year-old man who was found to have cecal carcinoma and later diagnosed with an IMT of the testis. IMTs are generally benign tumors with a tendency for local recurrence. Patients affected by IMTs usually get diagnosed only after more than one biopsy. IMT is diagnosed only after ruling out other differential diagnoses. They rarely show invasiveness and metastasize. The presence of metastasis, recurrence, and other malignancies probably indicate poor prognosis and poor survival. The course of IMTs is usually benign, with good outcomes after surgery. IMTs have been known to recur, invade, or metastasize in sites such as paranasal sinuses, mediastinum, and the abdomen. In the case that we researched, vimentin and smooth muscle actin were strongly positive in the spindle-shaped cells, whereas anaplastic lymphoma kinase-1 was negative.

摘要

炎性肌纤维母细胞瘤(IMTs)是一种罕见的肿瘤,可归类于纤维炎性疾病。IMTs是在排除所有其他可被视为IMTs鉴别诊断的实体后才得以确诊。IMTs的显微镜检查显示多个肌纤维母细胞性梭形细胞,其周围有炎症。IMTs发展为恶性肿瘤的几率较小。以下病例是文献中少数报告IMT与另一种恶性肿瘤并存的病例之一。我们描述了一名72岁男性,他被发现患有盲肠癌,后来又被诊断出患有睾丸IMT。IMTs通常是良性肿瘤,有局部复发的倾向。受IMTs影响的患者通常在经过多次活检后才得以确诊。IMT只有在排除其他鉴别诊断后才能确诊。它们很少表现出侵袭性和转移。转移、复发和其他恶性肿瘤的存在可能预示预后不良和生存率低。IMTs的病程通常是良性的,手术后效果良好。已知IMTs会在鼻窦、纵隔和腹部等部位复发、侵袭或转移。在我们研究的病例中,波形蛋白和平滑肌肌动蛋白在梭形细胞中呈强阳性,而间变性淋巴瘤激酶-1呈阴性。

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