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Successful Treatment of Pyoderma Gangrenosum with Cryoglobulinemia and Hepatitis C

机译:寒球菌血症与丙型肝炎的成功治疗

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Patient: Male, 68 Final Diagnosis: Pyoderma gangrenosum Symptoms: Worsening lower extremity wound Medication: — Clinical Procedure: — Specialty: Infectious Diseases Objective: Rare disease Background: Pyoderma gangrenosum is a rare, ulcerative cutaneous condition that was first described by Brocq in 1916. This diagnosis is quite challenging as the histopathological findings are nonspecific. Pyoderma gangrenosum is usually associated with inflammatory bowel disease, leukemia, and hepatitis C. We describe a rare clinical case of a patient with hepatitis C (HCV), mixed cryoglubinemia, and pyoderma gangrenosum, which was successfully treated with prednisone in combination with the new antiviral medication ledipasvir/sofosbuvir. Case Report: A 68-year-old male with a history of untreated HCV presented to the clinic with a left lower extremity ulcer that had progressively worsened over 4 days after the patient sustained a minor trauma to the left lower extremity. Examination revealed a 2×3 cm purulent ulcer with an erythematous rim on medial aspect of his left lower leg. HCV viral load and genotype analysis revealed genotype 1A with polymerase chain reaction (PCR) showing viral counts of 9,506,048 and cryoglobulinemia. With a worsening and enlarging erythematous ulcer and failure of IV antibiotic therapy, the patient underwent skin biopsy, which showed acanthotic epidermis with superficial and deep perivascular lymphoplasmacytic dermatitis admixed with mild neutrophilic infiltrate. The patient was subsequently started on ledipasvir/sofosbuvir and prednisone with a high suspicion of pyoderma gangrenosum. At one-month follow-up at the hepatology clinic, the patient demonstrated a near resolution of the lower extremity ulcer with undetectable viral load. Conclusions: Pyoderma gangrenosum is an inflammatory process of unknown etiology, and establishing the correct diagnosis can be a difficult task. For this reason it is prudent for clinicians to consider Pyoderma gangrenosum in their differential diagnosis, especially in the setting of a nonhealing surgical wound or skin infection.
机译:患者:男,68岁最终诊断:坏疽性脓皮病症状:下肢伤口加重药物治疗:—临床过程:—专长:传染病目的:罕见疾病背景:坏疽性脓皮病是一种罕见的溃疡性皮肤病,Brocq于1916年首次描述了这种病由于组织病理学结果是非特异性的,因此该诊断非常具有挑战性。坏疽性脓皮病通常与炎症性肠病,白血病和丙型肝炎相关。我们描述了罕见的丙型肝炎(HCV),混合性低温润滑脂和坏疽性脓皮病患者的临床病例,该患者成功地用泼尼松联合新药治疗抗病毒药物ledipasvir /索非布韦。病例报告:一位68岁的男性,未经治疗的HCV病史出现在诊所,左下肢溃疡在患者遭受左下肢轻伤后4天内逐渐恶化。检查发现他的左小腿内侧有一个2×3厘米的化脓性溃疡,边缘有红斑。 HCV病毒载量和基因型分析显示具有聚合酶链反应(PCR)的基因型1A,显示病毒计数为9,506,048和冷球蛋白血症。随着红斑性溃疡的恶化和扩大以及静脉注射抗生素治疗的失败,患者进行了皮肤活检,表现为棘皮表皮,浅表和深部血管周淋巴浆细胞性皮炎以及轻度中性粒细胞浸润。该患者随后开始接受高剂量怀疑有坏疽性脓皮病的ledipasvir / sofosbuvir和泼尼松治疗。在肝病门诊进行了一个月的随访,该患者表现出下肢溃疡的近乎消退的症状,并没有检测到病毒载量。结论:坏疽性脓皮病是一种病因不明的炎症过程,建立正确的诊断可能是一项艰巨的任务。因此,临床医生在鉴别诊断时应考虑坏疽性脓皮病,特别是在手术伤口不愈合或皮肤感染的情况下。

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