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远端指骨骨样骨瘤:一种罕见病症。

Osteoid Osteoma of the Distal Phalanx: A Rare Condition.

作者信息

Daher Jimmy C, Boushnak Mohammad O, Al Najjar Elie N, Tannoury Esther H, Moucharafieh Ramzi C

机构信息

Orthopedic Surgery, Lebanese American University Medical Center, Beirut, LBN.

Orthopedic Surgery, Lebanese University Faculty of Medicine, Beirut, LBN.

出版信息

Cureus. 2021 Oct 27;13(10):e19077. doi: 10.7759/cureus.19077. eCollection 2021 Oct.

Abstract

Osteoid osteoma of the distal phalanges in the hand is rare and difficult to diagnose. We report a case of a 37-year-old Caucasian female patient who presented with a mass on the distal phalanx of the index finger. The patient was suffering from intermittent nocturnal pain for more than 18 months along with thickening, localized swelling, and clubbing of the distal phalanx of the right index finger. Radiographs revealed a lytic lesion of the distal phalanx of the right index finger with surrounding sclerosis. An MRI showed an intramedullary lesion with infiltration of the bone marrow, cortex, and surrounding tissue with focal sclerosis and elements of enhancements. A presumptive diagnosis of osteoid osteoma was made and surgical removal of the lesion by curettage and bone grafting was the treatment of choice. The curetted specimen was sent to pathology and the diagnosis of osteoid osteoma was confirmed. The patient was asymptomatic at six months postoperatively. Osteoid osteoma should be included in every differential diagnosis for patients presenting with atypical features of the distal phalanx of the hand.

摘要

手部远节指骨骨样骨瘤罕见且诊断困难。我们报告一例37岁的白种女性患者,其示指远节指骨出现肿物。患者间歇性夜间疼痛超过18个月,同时伴有右手示指远节指骨增厚、局限性肿胀和杵状指。X线片显示右手示指远节指骨有溶骨性病变并伴有周围硬化。磁共振成像显示骨髓内病变,骨髓、皮质及周围组织有浸润,伴有局灶性硬化和强化表现。初步诊断为骨样骨瘤,治疗选择为刮除病变并植骨的手术切除。刮除的标本送去做病理检查,确诊为骨样骨瘤。术后6个月患者无症状。对于手部远节指骨出现非典型特征的患者,鉴别诊断时应考虑骨样骨瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5202/8610437/adf221d7bf9a/cureus-0013-00000019077-i06.jpg

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