Elsiesy Hussien, Saad Mohamed, Shorman Mahmoud, Amr Samir, Abaalkhail Faisal, Hashim Almoutaz, Al Hamoudi Waleed, Al Sebayel Mohamed, Selim Khalid
Department of Liver Transplantation, King Faisal Specialist Hospital and RC, Riyadh, Saudi Arabia.
Hepat Mon. 2013 Aug 11;13(8):e10858. doi: 10.5812/hepatmon.10858. eCollection 2013.
Cutaneous Mucormycosis is a rare opportunistic infection caused by Zygomycetes class of fungi that is often fatal, requiring aggressive local control as well as systemic therapy. Few cases of mucormycosis were described in patients with liver cirrhosis, mostly rhino-orbital. To our knowledge, only two cases of upper extremity involvement was reported in cirrhosis while a few cases were reported in the post-transplant setting. We report herein the third case of upper extremity mucor infection in the setting of liver cirrhosis.
We described a rare case of forearm infection originating in a traumatic intravenous access portal in a 25 year-old woman with liver cirrhosis secondary to autoimmune hepatitis.
She developed acute on chronic liver failure during the last trimester of pregnancy, which was terminated. Painful, erythematous lesion was noted on her right forearm in the area of intravenous access, which later became necrotic. Extensive debridement was done and histopathological examination confirmed the diagnosis of mucormycosis. The patient started on Amphotericin B. Her condition continued to deteriorate and ended up with above elbow amputation followed by right shoulder disarticulation. She died two days later due to multi-organ failure. In conclusion, forearm mucromycosis in liver cirrhosis can be fatal.
皮肤毛霉病是一种由接合菌纲真菌引起的罕见机会性感染,通常是致命的,需要积极的局部控制以及全身治疗。肝硬化患者中毛霉病的病例很少被描述,主要是鼻眶部感染。据我们所知,肝硬化患者中仅有两例上肢受累的报道,而在移植后患者中有少数病例报道。我们在此报告肝硬化患者中第三例上肢毛霉感染病例。
我们描述了一例罕见的前臂感染病例,该病例起源于一名25岁患有自身免疫性肝炎继发肝硬化的女性患者的创伤性静脉通路部位。
她在妊娠晚期出现急性慢性肝功能衰竭,随后终止妊娠。在其右前臂静脉通路部位发现疼痛性红斑病变,随后病变坏死。进行了广泛的清创术,组织病理学检查确诊为毛霉病。患者开始使用两性霉素B治疗。她的病情持续恶化,最终进行了肘上截肢,随后进行了右肩关节离断术。两天后,她因多器官衰竭死亡。总之,肝硬化患者的前臂毛霉病可能是致命的。