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毛母质癌:一种具有恶性后果的良性模仿者——病例报告及当前文献综述

Pilomatrix Carcinoma: A Benign-Mimic with Malignant Consequences - A Case Report and Review of the Current Literature.

作者信息

Slovacek Cedar A, Li Yang, Hurley Maria, Beshad Ramona, Bernstein Michael L

机构信息

Division of Plastic Surgery, Saint Louis University, St. Louis, MO, USA.

Department of Dermatology, Saint Louis University, St. Louis, MO, USA.

出版信息

Case Rep Dermatol. 2024 Jun 18;16(1):156-163. doi: 10.1159/000539123. eCollection 2024 Jan-Dec.

Abstract

INTRODUCTION

Pilomatrix carcinomas (PMXCs) are uncommon, locally aggressive tumors with high recurrence rates, metastatic potential, and fewer than 130 cases reported in the literature. Typically, they present as an unassuming, firm, dermal swelling and therefore are frequently mistaken for more common, benign masses, leading to undertreatment which can cause local invasion and metastatic spread. Diagnosis relies on excision with pathologic analysis; however once diagnosed, there are no current recommendations to guide treatment or surveillance for recurrence or metastases.

CASE PRESENTATION

Here, we present a case of one of these rare tumors. Our case describes a 1.5 × 2.5 cm firm, mobile mass at the supraorbital rim in an otherwise healthy, young patient. Prior to removal, we suspected a benign pathology; however, excision proved difficult and pathologic diagnosis was consistent with PMXC. Following discussion with tumor board, decision was made to perform Mohs micrographic surgery and staging via CT scans with regular follow-up and surveillance scans.

CONCLUSION

PMXCs are exceedingly rare diagnoses and present like many benign lesions. Therefore, we elected to document this case to encourage providers to keep these biologically aggressive tumors on their list of differential diagnoses in an unsuspecting mass, as well as to provide our own recommendations for treatment and screening for recurrence and metastatic spread.

摘要

引言

毛发基质癌(PMXC)是一种罕见的、具有局部侵袭性的肿瘤,复发率高,有转移潜能,文献报道的病例不足130例。通常情况下,它们表现为一个不起眼的、质地坚硬的皮肤肿物,因此常被误认为是更常见的良性肿块,导致治疗不足,进而引发局部侵袭和转移扩散。诊断依赖于切除并进行病理分析;然而,一旦确诊,目前尚无指导治疗或监测复发及转移的建议。

病例报告

在此,我们报告一例这种罕见肿瘤的病例。我们的病例描述的是一名健康年轻患者眶上缘处一个1.5×2.5厘米大小、质地坚硬、可活动的肿块。在切除之前,我们怀疑是良性病变;然而,切除过程困难,病理诊断与毛发基质癌一致。在与肿瘤委员会讨论后,决定进行莫氏显微外科手术,并通过CT扫描进行分期,同时定期进行随访和监测扫描。

结论

毛发基质癌的诊断极为罕见,且表现与许多良性病变相似。因此,我们选择记录此病例,以鼓励医疗人员在面对一个看似无害的肿块时,将这些具有生物学侵袭性的肿瘤列入鉴别诊断清单,同时提供我们自己对于治疗以及复发和转移扩散筛查的建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b975/11250398/ea164b50f27e/cde-2024-0016-0001-539123_F01.jpg

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