Pathological Hip Dislocation in a Neurofibromatosis Patient Secondary to Capsular Hemangioma

IF 1.1 4区 医学 Q3 ORTHOPEDICS
Badaruddin Sahito, Muhammad Waqas Khan, Muhammad Hamdan, Ushna Sunain Ansari, Awais Abro, Bakht Hussain, Maratib Ali
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引用次数: 0

Abstract

Neurofibromatosis is an autosomal-dominant multi-system disease affecting the nervous, integumentary, ocular, and musculoskeletal systems. In the small number of reported cases, the cause was either atraumatic or an intra-articular neurofibroma. Only a couple of articles in medical literature have reported synovial and capsular hemangioma originating within the hip joint. In this article, we present a rare case of pathological hip dislocation in a neurofibromatosis patient secondary to capsular hemangioma that would be reported for the first time in medical literature. We present the case of a 20-year-old female, resident of Karachi, who presented to the outpatient clinic with pain in the left hip join and inability to bear weight on left leg for 1 week. Diagnosed as a case of posterior hip dislocation after physical examination and imaging, her dislocation was reduced by the Allis method. This maneuver, however, was unsuccessful. Ultimately, the joint was reduced with open reduction via Steinmann pin because post-reduction hip joint was unstable to be contained into the acetabulum; therefore, Steinmann pin was used. The biopsy specimen taken from joint capsule and femoral neck during the surgery revealed cavernous hemangioma within the capsule. Hence, the etiology of posterior hip dislocation was attributed to the presence of capsular hemangioma within the hip joint. The surgery proved successful. The patient had remarkable recovery. The Steinmann pin was removed at 6 weeks, full weight-bearing started at 3 months, and range of motion extended from 0 to 90 degrees at 1 year with imaging studies showing a normally placed hip joint. The presented case reports an unusual etiology of a rare pathology occurring in association with a common genetic disease. It focuses on the importance of thorough examination and extensive relevant investigations in patients presenting with rare pathologies. These practices not only expedite the diagnosis and treatment of such patients, but can also reveal unusual etiologies responsible for uncommon pathologies. This case would help widen the differential diagnosis and treatment strategies of the physicians while dealing with neurofibromatosis patients with pathological hip dislocation.

Level of Evidence This is a case report having Level of Evidence 4 in accordance with the levels developed by the Centre of Evidence Based Medicine (CEBM) for treatment.

Graphical abstract

Abstract Image

一名神经纤维瘤病患者继发于囊状血管瘤的病理性髋关节脱位
神经纤维瘤病是一种常染色体显性遗传的多系统疾病,影响神经、皮肤、眼睛和肌肉骨骼系统。在少数报道的病例中,病因要么是非创伤性的,要么是关节内神经纤维瘤。医学文献中仅有几篇文章报道了起源于髋关节内的滑膜和关节囊血管瘤。在本文中,我们将首次在医学文献中报道一例神经纤维瘤病患者因囊状血管瘤继发病理性髋关节脱位的罕见病例。我们报告的病例是一名居住在卡拉奇的 20 岁女性患者,她因左髋关节疼痛和左腿无法负重一周而到门诊就诊。经过体格检查和影像学检查,她被诊断为髋关节后脱位。然而,这种方法并不成功。最后,由于还原后的髋关节不稳定,无法嵌入髋臼,因此使用了 Steinmann 销钉进行开放性还原。手术中从关节囊和股骨颈处提取的活检标本显示,关节囊内有海绵状血管瘤。因此,髋关节后脱位的病因被归结为髋关节内存在囊状血管瘤。手术非常成功。患者恢复良好。6 周后拔除了 Steinmann 针,3 个月后开始完全负重,1 年后活动范围从 0 度扩大到 90 度,影像学检查显示髋关节位置正常。本病例报告了一种与常见遗传病相关的罕见病变的不寻常病因。该病例强调了对罕见病症患者进行全面检查和广泛相关检查的重要性。这些做法不仅能加快对此类患者的诊断和治疗,还能揭示导致罕见病症的不寻常病因。本病例有助于医生在处理神经纤维瘤病患者的病理髋关节脱位时,扩大鉴别诊断和治疗策略的范围。
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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
185
审稿时长
9 months
期刊介绍: IJO welcomes articles that contribute to Orthopaedic knowledge from India and overseas. We publish articles dealing with clinical orthopaedics and basic research in orthopaedic surgery. Articles are accepted only for exclusive publication in the Indian Journal of Orthopaedics. Previously published articles, articles which are in peer-reviewed electronic publications in other journals, are not accepted by the Journal. Published articles and illustrations become the property of the Journal. The copyright remains with the journal. Studies must be carried out in accordance with World Medical Association Declaration of Helsinki.
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