巨型柔毛瘤并存血管肌瘤样基质组织病理学:一份病例报告

Francesca Mazzarella, Bianca Maria Del Forno, Enrico Caporali, A. Costa, Vincenzo Vindigni, F. Bassetto, T. Brambullo
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摘要

毛囊瘤又称马勒贝良性钙化上皮瘤,是一种起源于毛囊基质细胞的毛囊肿瘤。它通常表现为皮下坚实肿块,大小不超过 3 厘米。较少见的是,它的大小可能超过 5 厘米,在这种情况下被称为巨型毛囊瘤。我们在此介绍一例皮下病变,该病变具有侵袭性生物学行为,最初被认为是恶性的,但后来发现是一种罕见的血管肌瘤变异型巨型柔毛瘤。 该病例涉及一名年轻、健康的女性,她的右臂远外侧皮下病变生长迅速。经切口活检,病变被诊断为表皮和皮下组织增生,很可能是反应性增生。根治性切除后,病理学家对整个标本进行了分析,诊断出这是一种罕见的变异型巨大柔毛瘤,伴有血管肌瘤样基质。 典型的柔毛瘤是一种惰性、生长缓慢的病变,轮廓清晰,与下层组织平面不固定。然而,本病例中的皮损在 6 个月没有增大迹象后,开始以一种非常不寻常和令人担忧的方式生长,提示为皮肤恶性肿瘤。患者年龄较小,皮损发展迅速且面积较大,因此我们怀疑是肉瘤。 本病例强调了皮肤外科医生和病理学家之间合作的重要性,以确保对此类误导性病例进行彻底评估。这种合作将为适当的治疗决策提供指导,并避免对良性病变的过度治疗。
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Giant pilomatricoma with coexisting angiomyxoid stroma histopathology: a case report
Pilomatricoma, also known as benign calcifying epithelioma of Malherbe, is a follicular tumor originating from cells in the hair follicle matrix. It usually manifests as a firm subcutaneous mass up to 3 cm in size. Less commonly, it may measure >5 cm and in such cases is called giant pilomatricoma. We herein present a case of a subcutaneous lesion that was characterized by aggressive biological behavior and initially thought to be malignant but subsequently found to be a rare angiomyxoid variant of giant pilomatricoma. This case involved a young, healthy woman with a rapidly growing subcutaneous lesion on the distal lateral side of her right arm. An incisional biopsy was performed, and the lesion was diagnosed as hyperplasia of the epidermis and subcutaneous tissue, likely of reactive nature. After radical excision, analysis of the entire specimen led the pathologist to diagnose a rare variant of giant pilomatricoma with angiomyxoid stroma. Classic pilomatricoma is an indolent, slow-growing lesion that is well defined and not fixed to the underlying tissue planes. However, after showing no signs of enlargement for 6 months, the lesion in the present case began to grow in a very unusual and concerning manner, suggesting a skin malignancy. The patient’s young age and the rapid development and large dimensions of the lesion led us to suspect a sarcoma. This case highlights the importance of cooperation between the dermatosurgeon and the pathologist to ensure thorough evaluation of such misleading cases. Such cooperation will guide appropriate management decisions and avoid overtreatment of benign lesions.
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