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巨大型出血性转子滑囊炎酷似高级别软组织肉瘤:两例报告。

Giant hemorrhagic trochanteric bursitis mimicking a high-grade soft tissue sarcoma: report of two cases.

机构信息

Rizzoli-Sicilia Department, IRCCS Istituto Ortopedico Rizzoli.

IRCCS Istituto Ortopedico Rizzoli.

出版信息

Acta Biomed. 2021 Apr 30;92(S1):e2021043. doi: 10.23750/abm.v92iS1.9151.

DOI:10.23750/abm.v92iS1.9151
PMID:33944848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8142766/
Abstract

BACKGROUND

The giant haemorrhagic bursitis of the hip joint is a rare clinical condition that requires evidence-based guidelines for adequate diagnosis and management. Usually, this pathology requires conservative treatment; however, when abnormal size or clinical symptoms of compression of the surrounding noble structures are reported, an accurate differential diagnosis is required, in order to exclude other malignant conditions that can be included into differential diagnosis, and a surgical approach should be considered. The purpose of this work is to provide an appropriate description of the diagnostic and therapeutic path, providing an accurate analysis of the possible differential diagnoses.

METHODS

We report 2 cases of symptomatic haemorrhagic bursitis of the hip joint, confirmed by histological investigation. In both cases, the patients complained a peripheral nerve deficit of a single limb: one patient presented paresthesia of lateral femoral cutaneous nerve while the second peripheral edema due to compression of the proximal venous and lymphatic circulation.

RESULTS

Both cases were successfully managed by complete surgical excision of the mass, with no  recurrence. There were no major complications, but in first case the nerve deficit was permanent.

CONCLUSIONS

Giant hemorrhagic trochanteric bursitis is a rare condition, but it should be included in the differential diagnosis of soft tissue masses arising from the hip joint. Due to the rarity of this entity, a cautious exclusion process of all plausible differential diagnosis must be undertaken, in order to not miss the possibility of soft-tissue tumors, primarily malignant high-grade sarcomas.

摘要

背景

髋关节巨大血肿性滑囊炎是一种罕见的临床情况,需要有循证医学指南来进行充分的诊断和管理。通常,这种病理需要保守治疗;然而,当报告有异常大小或周围重要结构受压的临床症状时,需要进行准确的鉴别诊断,以排除可能被误诊的其他恶性疾病,并应考虑手术治疗。本研究旨在提供一个合适的诊断和治疗路径描述,并对可能的鉴别诊断进行准确的分析。

方法

我们报告了 2 例经组织学证实的髋关节症状性血肿性滑囊炎病例。在这两种情况下,患者均出现单肢周围神经缺损:1 例患者出现股外侧皮神经感觉异常,另 1 例患者因近端静脉和淋巴循环受压而出现周围水肿。

结果

这 2 例患者均通过完全切除肿块成功治疗,且无复发。无重大并发症,但第 1 例患者的神经缺损是永久性的。

结论

巨大髋关节血肿性滑囊炎较为罕见,但应包括髋关节软组织肿块的鉴别诊断。由于这种疾病的罕见性,必须对所有可能的鉴别诊断进行谨慎的排除过程,以避免错过软组织肿瘤,尤其是恶性高级别肉瘤的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/8151120e0122/ACTA-92-43-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/b27c3aff1ecb/ACTA-92-43-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/e174378b4e19/ACTA-92-43-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/c71ef26c551d/ACTA-92-43-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/8151120e0122/ACTA-92-43-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/b27c3aff1ecb/ACTA-92-43-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/e174378b4e19/ACTA-92-43-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/c71ef26c551d/ACTA-92-43-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e0/8142766/8151120e0122/ACTA-92-43-g004.jpg

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Synovial cysts of the hip joint: a single-center experience.髋关节滑膜囊肿:单中心经验
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Huge Bursitis and Bursal Synovial Osteochondromatosis Associated With Scapular Osteochondroma Mimicking a Giant Calcific Mass of the Chest Wall.巨大滑囊炎和滑囊滑膜骨软骨瘤病伴肩胛软骨瘤,类似于胸壁巨大钙化肿块。
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Synovial cysts of the hip.髋关节滑膜囊肿
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Common Superficial Bursitis.常见浅表滑囊炎
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