Choy Carolyn, Cooper Alan, Kossard Steven
Skin and Cancer Foundation Australia, Darlinghurst, New South Wales, Australia.
Australas J Dermatol. 2006 Nov;47(4):291-5. doi: 10.1111/j.1440-0960.2006.00298.x.
A 65-year-old man presented with an indurated plaque over his left cheek and left neck. An initial punch biopsy of skin showing increased smooth muscle bundles was consistent with a diagnosis of smooth muscle hamartoma. A second incisional skin biopsy revealed a well-differentiated smooth muscle proliferation invading into the dermis and subcutaneous fat in a diffusely infiltrative pattern and with a desmoplastic component, suggesting a diagnosis of desmoplastic leiomyosarcoma. Resection of the tumour confirmed the presence of a cytologically low grade leiomyosarcoma with an insidious infiltrative growth pattern. This rare pattern of diffuse leiomyosarcoma is important to recognize as the histological features are subtle and may potentially constitute a pitfall in histological diagnosis in a small biopsy specimen. In addition, our case illustrates overlapping morphology between diffuse and desmoplastic types of leiomyosarcoma.
一名65岁男性患者,左侧脸颊和颈部出现硬结性斑块。最初的皮肤穿刺活检显示平滑肌束增多,符合平滑肌错构瘤的诊断。第二次皮肤切开活检显示,高分化平滑肌增生以弥漫浸润性方式侵入真皮和皮下脂肪,并伴有促纤维增生成分,提示促纤维增生性平滑肌肉瘤的诊断。肿瘤切除证实存在细胞学低级别平滑肌肉瘤,具有隐匿性浸润性生长模式。这种罕见的弥漫性平滑肌肉瘤模式很重要,因为其组织学特征不明显,在小活检标本的组织学诊断中可能构成陷阱。此外,我们的病例说明了弥漫性和平滑肌促纤维增生性平滑肌肉瘤之间的形态学重叠。