Department of Radiation Oncology, St. Luke's Hospital, Dublin, Ireland.
Diagn Pathol. 2008 Nov 29;3:47. doi: 10.1186/1746-1596-3-47.
Pilomatrix carcinoma is the rare malignant counterpart of pilomatrixoma, a skin adnexal tumour originating from hair matrix cells. Pilomatrix carcinoma can arise as a solitary lesion de novo, or through transformation of a pilomatrixoma. Pilomatrixoma was first described erroneously as being of sebaceous gland origin but was later discovered to be derived from hair matrix cells. They are rare, slow growing tumours of the skin found in the lower dermis and subcutaneous fat and are predominantly found in the neck and the scalp. While known to be locally aggressive, no malignant form was thought to exist until it was described relatively recently. Since then, approximately ninety cases of pilomatrix carcinoma have been reported.We report the case of a 41 year old mentally retarded male who had a longstanding lesion in the left neck for approximately fifteen years previously diagnosed as a pilomatrixoma. He presented with severe headache, falls and visual disturbance and a biopsy showed pilomatrix carcinoma of the occipital region which, on computed tomography ( CT ) invaded the occipital bone, the cerebellum and the left temporal lobe. At his initial presentation he had a craniotomy and subtotal excision of the lesion but received no adjuvant therapy. After an early intracranial recurrence he had further debulking and adjuvant external beam radiotherapy. He has had no further intracranial recurrence after three and a half years of follow-up. Here we present the pathological features of this uncommon tumour.
毛母质瘤是毛母质瘤的罕见恶性对应物,毛母质瘤是一种起源于毛发基质细胞的皮肤附属器肿瘤。毛母质癌可作为新的单一病变发生,也可通过毛母质瘤的转化发生。毛母质瘤最初被错误地描述为来源于皮脂腺,但后来发现它是由毛发基质细胞衍生而来的。它们是罕见的、生长缓慢的皮肤肿瘤,位于真皮下层和皮下脂肪中,主要见于颈部和头皮。虽然已知具有局部侵袭性,但在最近才描述出恶性形式之前,人们认为不存在恶性形式。此后,大约报告了 90 例毛母质癌病例。我们报告了一例 41 岁智力低下男性的病例,他在左颈部有一个长期存在的病变,大约 15 年前被诊断为毛母质瘤。他出现严重头痛、跌倒和视力障碍,活检显示枕部毛母质癌,在计算机断层扫描(CT)上侵犯枕骨、小脑和左侧颞叶。他最初就诊时接受了开颅术和病变的大部分切除术,但未接受辅助治疗。早期颅内复发后,他接受了进一步的减瘤和辅助外照射放疗。在 3 年半的随访后,他没有再出现颅内复发。在此,我们介绍了这种罕见肿瘤的病理特征。