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Anomalous flexor digitorum superficialis muscle belly presenting as a mass within the palm

机译:掌浅部出现异常屈肌指浅肌腹部

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摘要

Anomalies of the flexor digitorum superficialis muscle are extremely uncommon and usually present as a painful mass or pseudotumour within the palm. Diagnosis may be difficult because many other soft tissue tumours (lipomas, ganglions, giant cell tumours and hamartomas) may present similarly. Magnetic resonance imaging helps to define the extent and characteristics of this anomalous muscle belly and to distinguish it from a soft tissue sarcoma, whereas plain radiographs are of little value. Three types of flexor digitorum superficialis muscle anomalies have been described, and treatment consists of subtotal or total surgical debulking of the mass if symptoms persist or if the diagnosis is in question. Most patients have complete resolution and full recovery. To date, 20 cases have been reported in the literature, usually involving the right small finger. In the present paper, the case of an anomalous flexor digitorum superficialis muscle in a 17-year-old male patient’s left index finger is reported. Symptoms were relieved following surgical debulking and hand-based occupational therapy.
机译:浅指屈肌异常极少见,通常以手掌内疼痛性肿块或假瘤的形式出现。由于许多其他软组织肿瘤(脂肪瘤,神经节,巨细胞瘤和错构瘤)可能会相似地出现,因此诊断可能很困难。磁共振成像有助于确定异常肌肉腹部的程度和特征,并将其与软组织肉瘤区分开,而普通的X线照片几乎没有价值。已经描述了三种类型的浅指屈浅肌异常,并且如果症状持续或如果对诊断有疑问,则治疗包括对小块进行小计或全部手术。大多数患者可以完全解决并完全康复。迄今为止,文献中已报道20例,通常涉及右小指。本文报道了一名17岁男性患者左手食指的屈指浅肌弯曲异常的情况。手术减量和以手为基础的职业治疗后,症状得到缓解。

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