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在长期朗格汉斯细胞组织细胞增多症背景下及近期使用达拉非尼治疗后出现的腹直肌坏死性肌炎。

Necrotizing myositis in a rectus muscle arising in the setting of long-standing Langerhans cell histiocystosis and recent dabrafenib treatment.

作者信息

van Landingham Suzanne W, Puccetti Diane, Potter Heather, Gamm David, Diamond Eli L, Lucarelli Mark J

机构信息

Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison, 2828 University Avenue, Madison, WI, 53705, USA.

Department of Pediatrics, American Family Children's Hospital University of Wisconsin-Madison, 1675 Highland Avenue, Madison, WI, 53792, USA.

出版信息

Am J Ophthalmol Case Rep. 2020 Aug 13;20:100868. doi: 10.1016/j.ajoc.2020.100868. eCollection 2020 Dec.

Abstract

PURPOSE

to describe an unusual case of necrotizing myositis in a rectus muscle, possibly related to BRAF inhibitor therapy.

OBSERVATIONS

An 18-year old man with neurodegenerative Langerhans cell histiocytosis (LCH), recently started on the BRAF inhibitor dabrafenib, presented with right eye pain. Magnetic resonance imaging (MRI) orbits revealed a rectus muscle mass concerning for LCH recurrence or malignancy. Dabrafenib was stopped, and incisional biopsy of the mass was performed. The mass was absent on post-operative MRI, so no further treatment was pursued. Histopathologic evaluation was initially concerning for sarcoma, but on further analysis, appeared more consistent with necrotizing myositis. The mass did not recur, nor did the patient develop other signs or symptoms concerning for myositis or malignancy over a 24-month follow-up period.

CONCLUSIONS

Necrotizing myositis has not been previously described in a rectus muscle or with BRAF inhibitor use, though myalgias and malignancies are established side effects. Necrotizing myositis may masquerade as sarcoma and should be on the differential diagnosis for a new mass in the setting of dabrafenib therapy.

摘要

目的

描述一例罕见的直肌坏死性肌炎病例,可能与BRAF抑制剂治疗有关。

观察结果

一名患有神经退行性朗格汉斯细胞组织细胞增多症(LCH)的18岁男性,最近开始使用BRAF抑制剂达拉非尼,出现右眼疼痛。眼眶磁共振成像(MRI)显示直肌肿块,怀疑为LCH复发或恶性肿瘤。停用达拉非尼,并对肿块进行切开活检。术后MRI显示肿块消失,因此未进行进一步治疗。组织病理学评估最初怀疑为肉瘤,但进一步分析后,似乎更符合坏死性肌炎。在24个月的随访期内,肿块未复发,患者也未出现其他与肌炎或恶性肿瘤相关的体征或症状。

结论

尽管肌痛和恶性肿瘤是已确定的副作用,但之前尚未有关于直肌坏死性肌炎或使用BRAF抑制剂导致坏死性肌炎的描述。坏死性肌炎可能会伪装成肉瘤,在达拉非尼治疗的情况下,应作为新肿块鉴别诊断的考虑因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f45/7452147/19a9d2f0ffb5/gr1.jpg

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