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[罕见原发性皮肤癌的不寻常定位:病例报告]

[Unusual localisation of rare primary skin carcinoma: a case report].

作者信息

Elousrouti Layla Tahiri, Bentayeb Rafik, Douida Amal, Abid Hakima, Abraki Mohamed, Ibrahimi Adil, Elloudi Sara, Baybay Hanane, Elmernissi Fatimazahra, Lamrani Youssef Alaoui, Hammas Nawal, Elfatemi Hinde, Chbani Laila

机构信息

Laboratoire d´Anatomie et de Cytologie Pathologiques, Centre Hospitalier Universitaire Hassan II de Fès, Fès, Maroc.

Laboratoire de Recherche Biomédicale et Translationnelle, Faculté de Médecine et de Pharmacie, Université Sidi Mohammed Ben Abdellah, Fès, Maroc.

出版信息

Pan Afr Med J. 2022 Apr 22;41:329. doi: 10.11604/pamj.2022.41.329.28965. eCollection 2022.

DOI:10.11604/pamj.2022.41.329.28965
PMID:35865833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9269034/
Abstract

Adnexal carcinomas are rare, accounting for less than 1% of skin carcinomas. Sclerosus carcinoma of the sweat glands was first described by Goldstein et al. in 1982. We here report the case of a 33-year-old female patient with a retracted perianal skin lesion. Histological examination of perilesional skin biopsy, immunohistochemistry, and negative results of laboratory tests, radiological and endoscopic investigations allowed for the diagnosis of eccrine sclerosus carcinoma. This is a rare tumor, usually characterized by facial localization and slow but aggressive progression. It poses problems in differential diagnosis with benign and malignant tumors; hence the challenge encountered by pathologist of suspecting this carcinoma in patients with any sclerotic and infiltrating skin lesion characterized by slow progression, in a context of preservation of the general state and in the absence of neoplastic history as well as of feeling free to ask for new deep biopsies when in doubt.

摘要

附件癌很罕见,占皮肤癌的比例不到1%。汗腺硬化性癌于1982年由戈尔茨坦等人首次描述。我们在此报告一例33岁女性患者,其肛周皮肤病变回缩。对病变周围皮肤活检进行组织学检查、免疫组化检查,以及实验室检查、影像学和内镜检查的阴性结果,得以诊断为小汗腺硬化性癌。这是一种罕见的肿瘤,通常表现为面部定位,进展缓慢但具有侵袭性。它在与良性和恶性肿瘤的鉴别诊断中存在问题;因此,病理学家在面对任何以缓慢进展为特征的硬化性和浸润性皮肤病变患者时,在患者一般状况良好、无肿瘤病史且存疑时可自由要求进行新的深部活检的情况下,怀疑这种癌症会遇到挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/d71509f912de/PAMJ-41-329-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/e307dd40197a/PAMJ-41-329-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/feb32dbe4c2a/PAMJ-41-329-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/862f873edc9e/PAMJ-41-329-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/24445c39d5b2/PAMJ-41-329-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/68afc4f051f8/PAMJ-41-329-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/b3d0cc77c566/PAMJ-41-329-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/d71509f912de/PAMJ-41-329-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/e307dd40197a/PAMJ-41-329-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/feb32dbe4c2a/PAMJ-41-329-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/862f873edc9e/PAMJ-41-329-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/24445c39d5b2/PAMJ-41-329-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/68afc4f051f8/PAMJ-41-329-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/b3d0cc77c566/PAMJ-41-329-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff2/9269034/d71509f912de/PAMJ-41-329-g007.jpg

相似文献

1
[Unusual localisation of rare primary skin carcinoma: a case report].[罕见原发性皮肤癌的不寻常定位:病例报告]
Pan Afr Med J. 2022 Apr 22;41:329. doi: 10.11604/pamj.2022.41.329.28965. eCollection 2022.
2
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MRI of a microcystic adnexal carcinoma of the skin mimicking a fibrous tumour: case report and literature review.皮肤微囊性附属器癌的 MRI 表现酷似纤维瘤:病例报告及文献复习。
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Estrogen and progesterone receptors and anti-gross cystic disease fluid protein 15 (BRST-2) fail to distinguish metastatic breast carcinoma from eccrine neoplasms.雌激素和孕激素受体以及抗大汗腺囊肿病液体蛋白15(BRST-2)无法区分转移性乳腺癌和小汗腺肿瘤。
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[Eccrine carcinoma: a diagnostic pitfall].
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本文引用的文献

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Evidence-Based Clinical Practice Guidelines for Microcystic Adnexal Carcinoma: Informed by a Systematic Review.微囊性附件癌的循证临床实践指南:基于系统评价
JAMA Dermatol. 2019 Sep 1;155(9):1059-1068. doi: 10.1001/jamadermatol.2019.1251.
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Microcystic Adnexal Carcinoma: A Rare, Commonly Misdiagnosed Malignancy.微囊性附属器癌:一种罕见且常被误诊的恶性肿瘤。
Mil Med. 2019 Dec 1;184(11-12):948-950. doi: 10.1093/milmed/usz123.
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Microcystic Adnexal Carcinoma: A Review of the Literature.微囊性附属器癌:文献综述
Dermatol Surg. 2017 Aug;43(8):1012-1016. doi: 10.1097/DSS.0000000000001142.
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Microcystic adnexal carcinoma in a non-Caucasian patient: A case report and review of the literature.一名非白种人患者的微囊性附属器癌:病例报告及文献复习
Oncol Lett. 2016 Apr;11(4):2471-2474. doi: 10.3892/ol.2016.4242. Epub 2016 Feb 17.
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Diagnostic Immunohistochemistry in Cutaneous Neoplasia: An Update.皮肤肿瘤的诊断性免疫组织化学:最新进展
Dermatopathology (Basel). 2015 Apr 8;2(1):15-42. doi: 10.1159/000377698. eCollection 2015 Jan-Mar.
6
p63 Immunohistochemistry is a useful adjunct in distinguishing sclerosing cutaneous tumors.p63免疫组织化学在鉴别硬化性皮肤肿瘤方面是一种有用的辅助手段。
Am J Dermatopathol. 2010 May;32(3):257-261. doi: 10.1097/DAD.0b013e3181b7fc76.
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Microcystic adnexal carcinoma: forty-eight cases, their treatment, and their outcome.微囊性附属器癌:48例病例、治疗及预后
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Sclerosing sweat duct carcinoma in the peri-anal skin: a case report.肛周皮肤硬化性汗腺导管癌:一例报告
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Microcystic adnexal carcinoma: a distinct clinicopathologic entity.微囊性附属器癌:一种独特的临床病理实体。
Cancer. 1982 Aug 1;50(3):566-72. doi: 10.1002/1097-0142(19820801)50:3<566::aid-cncr2820500330>3.0.co;2-q.
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Sclerosing sweat duct (syringomatous) carcinoma.硬化性汗腺导管(汗腺瘤样)癌
Am J Surg Pathol. 1985 Jun;9(6):422-33. doi: 10.1097/00000478-198506000-00004.