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模仿鳞状细胞癌的增殖性坏疽性脓皮病:一个未得到充分认识的诊断挑战。

Vegetative Pyoderma Gangrenosum Mimicking Squamous Cell Carcinoma: A Poorly Recognized Diagnostic Challenge.

作者信息

Hoang Megan, Maymone Mayra B C, Telang Gladys H, Seo Su-Jean, Robinson-Bostom Leslie

机构信息

Warren Alpert Medical School of Brown University, Providence, RI; and.

Department of Dermatology, Warren Alpert Medical School of Brown University, Providence, RI.

出版信息

Am J Dermatopathol. 2025 Apr 1;47(4):e47-e49. doi: 10.1097/DAD.0000000000002919. Epub 2024 Dec 31.

DOI:10.1097/DAD.0000000000002919
PMID:39787338
Abstract

Pyoderma gangrenosum (PG) is a rare inflammatory neutrophilic dermatosis that is difficult to diagnose due to non-specific clinical, laboratory, and histopathologic features. Distinguishing pseudoepitheliomatous hyperplasia (PEH) from squamous cell carcinoma (SCC) is also histopathologically challenging. The connection between PEH and PG is not well recognized, and instances of PG mimicking SCC are rare. We report a case of vegetative PG accompanied by PEH, originally mistaken for SCC. A 78-year-old woman presented with a 3-month history of an ulcerated, exophytic, and painful mass on her right lower leg. An incisional biopsy revealed PEH and neutrophilic microabscesses, initially raising concerns for SCC keratoacanthoma type with PEH or well-differentiated, infiltrative SCC. However, following additional review of clinical and histopathologic findings at the cutaneous oncology tumor board, the diagnosis of vegetative PG with associated PEH was favored. This case highlights the significance of recognizing PEH as a histopathology feature that can be seen in PG and lead to difficulty distinguishing PG with PEH from SCC. We stress the importance of promptly diagnosing PG through clinical and histopathologic correlation to prevent diagnostic delays and unnecessary surgeries or treatments.

摘要

坏疽性脓皮病(PG)是一种罕见的炎症性嗜中性皮肤病,由于其临床、实验室和组织病理学特征不具特异性,故难以诊断。从组织病理学角度区分假上皮瘤样增生(PEH)和鳞状细胞癌(SCC)也具有挑战性。PEH与PG之间的联系尚未得到充分认识,且PG模仿SCC的病例较为罕见。我们报告一例伴有PEH的增殖性PG病例,最初被误诊为SCC。一名78岁女性,右小腿出现一个溃疡、外生性且疼痛的肿块,病程3个月。切开活检显示有PEH和嗜中性微脓肿,最初令人担心为伴有PEH的SCC角化棘皮瘤型或高分化浸润性SCC。然而,在皮肤肿瘤学肿瘤讨论会上对临床和组织病理学检查结果进行进一步评估后,倾向于诊断为伴有相关PEH的增殖性PG。该病例突出了认识到PEH是PG中可见的一种组织病理学特征,可导致难以将伴有PEH的PG与SCC区分开来的重要性。我们强调通过临床与组织病理学相互关联及时诊断PG的重要性,以防止诊断延误以及不必要的手术或治疗。

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