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颈部颗粒细胞瘤采用局部皮瓣治疗:病例报告。

Granular cell tumor of the neck treated using a local flap: A case report.

机构信息

Department of Otolaryngology-HNS, Seoul National University Hospital, Seoul, Korea.

Department of Otolaryngology-HNS, Research Institute for Clinical Medicine of Jeonbuk National University- Biomedical Research Institute of Jeonbuk National University Hospital, Jeonbuk, Korea.

出版信息

Medicine (Baltimore). 2023 Feb 22;102(8):e32641. doi: 10.1097/MD.0000000000032641.

Abstract

RATIONALE

Granular cell tumors are rare soft tissue neoplasms derived from nerve that can arise in the oral cavity, skin, or gastrointestinal tract. Various hypotheses have proposed that granular cell tumors originate from the nervous system, skeletal muscle, and Schwann cells.

PATIENT CONCERNS

A 47-year-old male patient presented with a 5 cm cervical mass.

DIAGNOSES

Computed tomography showed a 4 cm-sized homogeneous enhancing mass infiltrating the sternocleidomastoid muscle and even the surrounding skin.

INTERVENTIONS

Extensive surgical resection of the tumor including the skin was performed. A submental transposition local flap was used for the wide skin defect.

OUTCOMES

Histologic finding showed polygonal granular cells with rich eosinophilic coarse granular cytoplasm without interstitial tissue without mitosis or necrosis. Immunohistochemically, the tumor cells were positive for S100 and CD68, which is consistent with classic granular cell tumors.

LESSONS

In microscopic observations, granular cell tumors do not have a defined boundary with surrounding tissues, and they display an infiltrating pattern that can expand to adjacent tissue. As a result, the tumor should be removed with a sufficient margin, including the normal tissues surrounding it. The authors experienced granular cell tumor in the muscle layer of the head and neck. It could be treated without recurrence through extensive surgical resection and local flap.

摘要

背景

颗粒细胞瘤是一种罕见的来源于神经的软组织肿瘤,可发生于口腔、皮肤或胃肠道。各种假说提出,颗粒细胞瘤起源于神经系统、骨骼肌和施万细胞。

患者情况

一名 47 岁男性患者出现颈部长达 5cm 的肿块。

诊断

计算机断层扫描显示,一个 4cm 大小的均质强化肿块浸润胸锁乳突肌,甚至周围皮肤。

干预措施

广泛切除肿瘤,包括皮肤。采用颏下转位局部皮瓣修复广泛的皮肤缺损。

结果

组织学检查显示,多边形颗粒细胞具有丰富的嗜酸性粗颗粒细胞质,无间质组织,无有丝分裂或坏死。免疫组织化学检查显示,肿瘤细胞 S100 和 CD68 阳性,符合经典颗粒细胞瘤的特征。

教训

在显微镜下观察,颗粒细胞瘤与周围组织没有明确的界限,呈浸润性生长模式,可以扩展到邻近组织。因此,肿瘤应连同其周围正常组织一并切除,保证有足够的切缘。作者曾遇到过发生于头颈部肌肉层的颗粒细胞瘤,通过广泛的手术切除和局部皮瓣,肿瘤得到了无复发的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f076/11309720/b49636d40c64/medi-102-e32641-g001.jpg

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