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左大腿巨大原发性皮肤肌上皮癌伴腹股沟及盆腔淋巴结转移

Giant Primary Cutaneous Myoepithelial Carcinoma of the Left Thigh With Inguinal and Pelvic Lymph Node Metastases.

作者信息

Obata Ayaka, Kawahara Hikaru, Sugino Hitomi, Amagata Yoko, Saito-Sasaki Natsuko, Okada Etsuko, Sawada Yu

机构信息

Dermatology, University of Occupational and Environmental Health, Kitakyushu, JPN.

出版信息

Cureus. 2024 Sep 3;16(9):e68571. doi: 10.7759/cureus.68571. eCollection 2024 Sep.

DOI:10.7759/cureus.68571
PMID:39364518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11449504/
Abstract

Myoepithelial carcinoma is an exceedingly rare malignancy, particularly when originating from the skin. It frequently arises from malignant transformations of pleomorphic adenomas in various locations such as the parotid gland, breast, soft tissues, and lungs. Primary cutaneous myoepithelial carcinoma is exceptionally rare, often leading to delayed diagnosis. We report a case of giant primary cutaneous myoepithelial carcinoma of the left thigh, initially misdiagnosed as squamous cell carcinoma (SCC). The patient, a 64-year-old male, presented with a rapidly enlarging, ulcerated, and necrotic skin lesion. The initial presentation mimicked SCC. Due to the large tumor size and anemia caused by the tumor, the patient underwent a reduced-dose chemotherapy regimen (cytarabine plus aclarubicin chemotherapy) to shrink the tumor, enabling successful local surgical resection. Post-surgery, the patient received radiotherapy and tegafur gimeracil oteracil potassium, resulting in disease control without progression for two years. This case highlights the diagnostic challenges of myoepithelial carcinoma, which can mimic SCC among numerous other tumors. Accurate diagnosis relies on immunohistochemical staining and careful pathological evaluation. The case underscores the importance of considering myoepithelial carcinoma in the differential diagnosis of ulcerative tumors.

摘要

肌上皮癌是一种极为罕见的恶性肿瘤,尤其是起源于皮肤时。它常源于多形性腺瘤在腮腺、乳腺、软组织和肺等不同部位的恶性转化。原发性皮肤肌上皮癌极为罕见,常导致诊断延迟。我们报告一例左大腿巨大原发性皮肤肌上皮癌病例,最初被误诊为鳞状细胞癌(SCC)。患者为一名64岁男性,表现为迅速增大、溃疡和坏死的皮肤病变。最初的表现类似SCC。由于肿瘤体积大且导致贫血,患者接受了减量化疗方案(阿糖胞苷加阿柔比星化疗)以缩小肿瘤,从而得以成功进行局部手术切除。术后,患者接受了放疗和替吉奥,疾病得到控制,两年无进展。该病例突出了肌上皮癌的诊断挑战,它在众多其他肿瘤中可能类似SCC。准确诊断依赖免疫组化染色和仔细的病理评估。该病例强调了在溃疡性肿瘤鉴别诊断中考虑肌上皮癌的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/60b687ed5e34/cureus-0016-00000068571-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/3b6266cde258/cureus-0016-00000068571-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/257439a768ef/cureus-0016-00000068571-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/8925cbf4772a/cureus-0016-00000068571-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/60b687ed5e34/cureus-0016-00000068571-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/3b6266cde258/cureus-0016-00000068571-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/257439a768ef/cureus-0016-00000068571-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/8925cbf4772a/cureus-0016-00000068571-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e68/11449504/60b687ed5e34/cureus-0016-00000068571-i04.jpg

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本文引用的文献

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