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引起扳机指和间歇性腕管综合征的环指指深屈肌腱纤维脂肪瘤

Fibrolipoma of Flexor Digitorum Profundus Tendon of Ring Finger Causing Triggering and Intermittent Carpal Tunnel Syndrome.

作者信息

Sharma Bharati Pankaj Deokar, Sharma Pankaj Nandkishor

机构信息

Department of Orthopaedics, Symbiosis Medical College for Women, Pune, Maharashtra, India.

Department of Orthopaedics, Pad. Dr. D Y Patil Medical College, Hospital and Research Centre, Pimpri-Chinchwad, Maharashtra, India.

出版信息

J Orthop Case Rep. 2023 Jun;13(6):84-88. doi: 10.13107/jocr.2023.v13.i06.3706.

Abstract

INTRODUCTION

Lipomas are most common soft-tissue tumors but rarely are found to be symptomatic. <1% of lipomas are found in hand. Subfascial lipomas can cause pressure symptoms. Carpal tunnel syndrome (CTS) can be idiopathic or secondary to any space-occupying lesion. Triggering usually occurs due to inflammation/thickening of A1 pulley. Most have reported a lipoma in distal forearm or near median nerve, leading to triggering of index or middle finger and carpal tunnel symptoms. All the cases reported had either an intramuscular lipoma in flexor digitorum superficialis (FDS) tendon slip of index or middle finger, with or without accessory belly of FDS muscle or a neurofibrolipoma of the median nerve. In our case, the lipoma was under palmer fascia, in flexor digitorum profundus (FDP) tendon sheath of fourth finger causing triggering of the ring finger and CTS symptoms in flexion of the ring finger. Hence, this is a first report of this kind in the literature.

CASE REPORT

We hereby report a one of its kind case in which a 40-year-old Asian male patient had triggering of the ring finger with associated intermittent CTS symptoms, on making a fist, secondary to space-occupying lesion in palm, which was diagnosed by ultrasound as lipoma in FDP tendon of the ring finger in palm. This lipoma was surgically removed by AO ulnar palmer approach and carpal tunnel was decompressed. Histopathology report confirmed the lump to be fibrolipoma. The patient had complete relief of symptoms postoperatively. At 2 years follow-up, there was no recurrence.

摘要

引言

脂肪瘤是最常见的软组织肿瘤,但很少出现症状。手部脂肪瘤的发生率低于1%。筋膜下脂肪瘤可引起压迫症状。腕管综合征(CTS)可为特发性或继发于任何占位性病变。扳机指通常是由于A1滑车的炎症/增厚引起。大多数报道称脂肪瘤位于前臂远端或正中神经附近,导致示指或中指扳机指及腕管综合征症状。所有报道的病例均为示指或中指指浅屈肌腱束内的肌内脂肪瘤,伴或不伴有指浅屈肌副肌腹,或正中神经的神经纤维脂肪瘤。在我们的病例中,脂肪瘤位于手掌筋膜下,在环指指深屈肌腱鞘内,导致环指扳机指及环指屈曲时的腕管综合征症状。因此,这是文献中此类病例的首例报道。

病例报告

我们在此报告一例独特病例,一名40岁的亚洲男性患者,握拳时出现环指扳机指并伴有间歇性腕管综合征症状,继发于手掌占位性病变,经超声诊断为手掌环指指深屈肌腱内的脂肪瘤。通过AO尺侧掌侧入路手术切除该脂肪瘤并对腕管进行减压。组织病理学报告证实肿块为纤维脂肪瘤。患者术后症状完全缓解。随访2年,无复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fd/10308987/bc6114708dea/JOCR-13-84-g001.jpg

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