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治疗侵袭性脑罕见恶性汗腺肿瘤:病例报告及文献综述

Managing a Rare Malignant Sweat Gland Tumor Invading the Brain: Case Report and Literature Review.

作者信息

Jagannatha Aniruddha Tekkatte, Khan Mansoor A, Karanth Shrithi, Srikantha Umesh, Varma Ravi, Mahadevan Anita

机构信息

M S Ramaiah Institute of Neurosciences, M S Ramaiah Medical College, Karnataka, India.

Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS) Bengaluru, Karnataka, India.

出版信息

World Neurosurg. 2016 Feb;86:513.e1-7. doi: 10.1016/j.wneu.2015.09.042. Epub 2015 Sep 26.

Abstract

BACKGROUND

Malignant sweat gland adnexal tumors are rare with an incidence of 0.001%. Of these, clear cell hidradenocarcinoma is an extremely uncommon subtype that accounts for 6% of malignant eccrine sweat gland tumors. They occur commonly in the head, neck, and extremities. Although they have a propensity for local recurrence, intracranial extension with brain invasion is extremely rare.

CASE DESCRIPTION

We report a 76-year-old man with a large, recurring, ulcerated, fungating scalp swelling of 14 years who presented with focal seizures and drowsiness. Neuroimaging revealed a massive tumor arising from the scalp to invade the left parietal lobe and extending to the right side with occlusion of the superior sagittal sinus. The overlying parietal bone was lytic with a "moth-eaten" appearance. He underwent wide excision of the scalp lesion, near-total cerebral tumor decompression followed by titanium mesh cranioplasty, rotation flap reconstruction of the scalp, and adjuvant radiotherapy to the skull vault. Histopathology revealed clear cell hidradenocarcinoma. Whole-body positron emission tomography scan did not reveal any other lesion. At 24 months' follow-up, he remains recurrence free.

CONCLUSION

We report a rare indolent case of clear cell hidradenocarcinoma invading the brain, which was managed with near-total decompression and adjuvant radiotherapy. Intracranial extension in such aggressive tumors poses challenges in management, and regular neuroimaging surveillance is advised.

摘要

背景

恶性汗腺附属器肿瘤罕见,发病率为0.001%。其中,透明细胞汗腺癌是一种极为罕见的亚型,占恶性小汗腺肿瘤的6%。它们常见于头、颈和四肢。尽管它们易于局部复发,但颅内扩展并侵犯脑极为罕见。

病例描述

我们报告一名76岁男性,有一个14年的、反复出现的、溃疡型、蕈样头皮肿物,伴有局灶性癫痫发作和嗜睡。神经影像学检查显示一个巨大肿瘤起源于头皮,侵犯左侧顶叶并延伸至右侧,导致上矢状窦闭塞。上方的顶骨呈溶骨性,外观呈“虫蚀样”。他接受了头皮病变广泛切除、近全脑肿瘤减压,随后进行钛网颅骨成形术、头皮旋转皮瓣重建以及颅顶辅助放疗。组织病理学检查显示为透明细胞汗腺癌。全身正电子发射断层扫描未发现任何其他病变。随访24个月时,他无复发。

结论

我们报告了一例罕见的、侵袭脑的惰性透明细胞汗腺癌病例,通过近全减压和辅助放疗进行治疗。这种侵袭性肿瘤的颅内扩展给治疗带来挑战,建议进行定期神经影像学监测。

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