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Intraosseous Neurothekeoma of the Hand in a 16-year-old Boy

机译:一名16岁男孩的手骨内神经鞘瘤

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摘要

Soft-tissue tumors are rare in the pediatric population. First described in 1969 as myxoma of the nerve sheath, the neurothekeoma is a benign tumor lesion with presumable origin in the nerve sheath. It occurs mainly in female children and presents as a mass of slow, subcutaneous growth, asymptomatic and without alteration of the local pigmentation. It is predominantly located in the head, neck, and extremities of the upper limbs. This report presents the case of a 16-year-old male with a tumor mass originating from the nerve sheath in the 4 left metacarpal, intraosseous, and relapsed after previous surgical resection 2 years before this observation. A marginal resection of the tumor mass was performed on the distal region of the fourth metacarpal, followed by curettage of the proximal phalanx and filling with structural autologous bone graft. The patient maintained a favorable postoperative clinical evolution, without local pain or range of motion limitation in his fingers. Radiologically, a progressive trabecular filling of the proximal phalanx of the fourth metacarpal was observed. At 17 months of follow-up, the patient is asymptomatic and shows no signs of relapse. The description of this case serves to increase the familiarity with this rare pathology, and aid its diagnosis and treatment.
机译:软组织肿瘤在儿科人群中很少见。神经鞘瘤于1969年首次被描述为神经鞘膜粘液瘤,是一种良性肿瘤病变,可能起源于神经鞘膜。它主要发生在女童中,表现为大量缓慢的皮下生长,无症状,而局部色素没有改变。它主要位于上肢的头部,颈部和四肢。本报告介绍了一名16岁男性,其肿瘤块起源于4 左掌骨,骨内,在此观察前2年进行过先前的手术切除后复发。在第四掌骨的远端区域进行肿瘤块的边缘切除,然后刮除近端指骨并填充自体结构骨移植物。该患者术后临床进展良好,手指无局部疼痛或活动受限。放射学上,观察到第四掌骨近端指骨逐渐进行小梁充盈。在随访的17个月中,患者无症状,没有复发迹象。该病例的描述有助于增加对这种罕见病理的熟悉程度,并有助于其诊断和治疗。

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