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伏立康唑致一名手指疼痛伴结节患儿的骨膜炎:病例报告及文献复习

Voriconazole-induced periostitis in a child with finger pain and nodules: case report and literature review.

作者信息

Urakawa Hiroshi, Ikuta Kunihiro, Sakai Tomohisa, Koike Hiroshi, Fujito Takeo, Nishida Yoshihiro, Imagama Shiro

机构信息

Department of Advanced Medicine, Nagoya University Hospital, 65 Tsurumai, Showa-ku, Nagoya, 466-8560, Japan.

Department of Orthopaedic Surgery, Nagoya University Hospital, Nagoya, Japan.

出版信息

BMC Musculoskelet Disord. 2025 Aug 12;26(1):779. doi: 10.1186/s12891-025-09059-z.

Abstract

BACKGROUND

Voriconazole-induced periostitis is predominantly reported in adults, with pediatric cases being exceedingly rare.

CASE PRESENTATION

This report describes an 8-year-old boy with voriconazole-induced periostitis presenting with finger pain and nodules, initially suspected to be bone tumors. The patient had been on voriconazole for two years and seven months to treat Aspergillus pneumonia and had been hospitalized for six months due to chronic graft-versus-host disease following hematopoietic stem cell transplantation and total body irradiation for severe congenital neutropenia. The patient presented with a five-month history of pain and a one-month history of a mass in the middle finger of his right hand. Radiographs revealed bone formation outside the cortical bone in the proximal phalanx of the right middle finger and the distal ulna. Differential diagnoses included benign bone-forming tumors, such as osteochondroma post-total body irradiation, and bizarre parosteal osteochondromatous proliferation. The diagnosis of voriconazole-induced periostitis was confirmed as new sites of periostitis became apparent during the disease course.

CONCLUSIONS

Voriconazole-induced periostitis should be considered, even in pediatric patients, when multiple nodular periosteal reactions are observed in immunosuppressed patients undergoing long-term voriconazole therapy.

摘要

背景

伏立康唑引起的骨膜炎主要在成人中报道,儿科病例极为罕见。

病例报告

本报告描述了一名8岁男孩,患有伏立康唑引起的骨膜炎,表现为手指疼痛和结节,最初怀疑是骨肿瘤。该患者因治疗曲霉性肺炎服用伏立康唑两年零七个月,因严重先天性中性粒细胞减少症接受造血干细胞移植和全身照射后发生慢性移植物抗宿主病而住院六个月。患者有右手中指疼痛五个月和肿块一个月的病史。X线片显示右手中指近节指骨和尺骨远端皮质骨外有骨形成。鉴别诊断包括良性骨形成肿瘤,如全身照射后的骨软骨瘤,以及怪异的骨旁骨软骨瘤样增殖。随着病程中骨膜炎新部位的出现,伏立康唑引起的骨膜炎诊断得以证实。

结论

在接受长期伏立康唑治疗的免疫抑制患者中,当观察到多个结节性骨膜反应时,即使是儿科患者,也应考虑伏立康唑引起的骨膜炎。

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