Stephens Nicholas, Marques Eric, Livingston Christopher
Division of Plastic and Reconstructive Surgery, University of Texas - Houston Health Science Center, Houston, Texas, USA.
Can J Plast Surg. 2007 Spring;15(1):44-6. doi: 10.1177/229255030701500103.
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.
指浅屈肌异常极为罕见,通常表现为手掌内的疼痛性肿块或假瘤。诊断可能困难,因为许多其他软组织肿瘤(脂肪瘤、腱鞘囊肿、巨细胞瘤和错构瘤)可能有类似表现。磁共振成像有助于明确这种异常肌腹的范围和特征,并将其与软组织肉瘤区分开来,而普通X线片价值不大。已描述了三种指浅屈肌异常类型,若症状持续或诊断存疑,治疗包括对肿块进行次全或全切除。大多数患者可完全缓解并完全康复。迄今为止,文献报道了20例,通常累及右手小指。本文报道了一名17岁男性患者左手示指的指浅屈肌异常病例。手术切除肿块并进行手部职业治疗后症状缓解。