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用于治疗多发性硬化症的皮下注射干扰素β部位的小叶性脂膜炎在组织学上可酷似胰腺脂膜炎。一项12例病例的研究。

Lobular panniculitis at the site of subcutaneous interferon beta injections for the treatment of multiple sclerosis can histologically mimic pancreatic panniculitis. A study of 12 cases.

作者信息

Ball Nigel J, Cowan Bryce J, Hashimoto Stanley A

机构信息

Department of Pathology, The University of Britsih Columbia and Vancouver General Hospital, Vancouver, British Columbia, Canada.

出版信息

J Cutan Pathol. 2009 Mar;36(3):331-7. doi: 10.1111/j.1600-0560.2008.01019.x. Epub 2008 Aug 19.

Abstract

BACKGROUND

Thrombosis, mucinosis and necrosis are well-described complications of subcutaneous interferon beta injections.

METHODS

We report 12 incisional biopsies from subcutaneous interferon beta injection sites in 12 multiple sclerosis (MS) patients from a single neurologist's practice.

RESULTS

We identified abscesses (two cases) or induration (two cases) in acute clinical lesions and lipoatrophy (eight cases) in chronic lesions (biopsied over a year after symptom onset at injection sites). Biopsies from three acute lesions showed vascular thrombosis, dermal mucinosis, lobular neutrophilic panniculitis, necrosis, calcification and hemosiderin deposition (biopsied 2 weeks to 2 months after symptom onset). Two cases contained sterile abscesses. Five of the eight chronic cases presented as hard, indurated lipoatrophy with livedo reticularis. Their biopsies showed subcutaneous calcification and lipoatrophy. Biopsies from the early calcific suppurative and late calcific atrophic phases histologically resembled the early and late phases of subcutaneous saponification in pancreatic panniculitis.

CONCLUSIONS

Reactions at the site of subcutaneous interferon beta injections are common. Lipoatrophy can be clinically identified in 39 of 85 MS patients (46%) receiving subcutaneous interferon beta injections for 1 year or longer in our practice. A reaction to interferon should be considered in the differential diagnosis of biopsies that show features of pancreatic panniculitis.

摘要

背景

血栓形成、黏蛋白沉积症和坏死是皮下注射干扰素β的常见并发症。

方法

我们报告了来自一位神经科医生诊所的12例多发性硬化症(MS)患者皮下干扰素β注射部位的12次切口活检结果。

结果

我们在急性临床病变中发现了脓肿(2例)或硬结(2例),在慢性病变(在注射部位症状出现一年后进行活检)中发现了脂肪萎缩(8例)。3例急性病变的活检显示血管血栓形成、真皮黏蛋白沉积症、小叶性嗜中性脂膜炎、坏死、钙化和含铁血黄素沉积(在症状出现后2周-2个月进行活检)。2例含有无菌脓肿。8例慢性病例中有5例表现为伴有网状青斑的坚硬、硬结性脂肪萎缩。其活检显示皮下钙化和脂肪萎缩。早期钙化化脓期和晚期钙化萎缩期的活检在组织学上类似于胰腺脂膜炎皮下皂化的早期和晚期阶段。

结论

皮下注射干扰素β部位的反应很常见。在我们的实践中,85例接受皮下注射干扰素β1年或更长时间的MS患者中,有39例(46%)临床上可识别出脂肪萎缩。在对显示胰腺脂膜炎特征的活检进行鉴别诊断时,应考虑干扰素反应。

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