Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-Shinbashi, Minato-Ku, Tokyo, Japan.
Department of Pathology, The Jikei University School of Medicine, Tokyo, Japan.
BMC Nephrol. 2023 Jul 28;24(1):223. doi: 10.1186/s12882-023-03276-1.
Granulomatosis with polyangiitis (GPA) is characterized by necrotizing granulomatous vasculitis involving small-sized vessels in the upper airways, lower airways, and kidneys. Renal pathology is usually characterized by focal segmental necrotizing glomerulonephritis, which often leads to rapidly progressive renal failure. This type of renal involvement is usually unapparent on radiography. The presence of a renal mass in a patient with GPA, although extremely rare, is recognizable. Herein, we report a rare case of GPA presenting as a solitary renal mass and present a review of the literature.
A 75-year-old woman presented with a solitary right kidney mass measuring 4 × 3.5 cm detected by enhanced computed tomography. There was no history of sinusitis, rhinitis, cough, or pneumonia suggestive of systemic GPA. Nephrectomy was performed based on the suspicion of renal cell carcinoma or malignant lymphoma. Three months later, she was admitted because her serum creatinine levels increased from 54.81 μmol/L to 405.76 μmol/L accompanied by a high C-reactive protein level of 159 mg/L. Anti-neutrophil cytoplasmic antibodies against myeloperoxidase and anti-proteinase 3 were negative. Histological examinations of the solitary renal mass revealed necrotizing granulomatous arteritis in the cortex and medullary vasa recta, surrounded by interstitial fibrosis, and focal segmental necrotizing glomerulonephritis in the localized lesion; however, signs of vasculitis were not observed in areas other than the solitary mass. Therefore, the patient was diagnosed with granulomatosis with polyangiitis (GPA). Despite treatment with prednisolone (30 mg/day), the patient developed oliguria with an elevation of her serum creatinine level to 583.44 μmol/L, which required hemodialysis within one month after the initiation of steroid therapy. The patient could successfully discontinue hemodialysis 21 months later, following a decrease in her serum creatinine level to 251.06 μmol/L.
GPA should be considered as one of the differential diagnoses of a solitary renal mass. Furthermore, patients with solitary renal masses associated with GPA may exhibit a favorable response to steroid or immunosuppressive treatment.
肉芽肿性多血管炎(GPA)的特征是坏死性肉芽肿性小血管炎累及上呼吸道、下呼吸道和肾脏的小血管。肾脏病理通常表现为局灶节段坏死性肾小球肾炎,常导致进行性肾功能衰竭。这种类型的肾受累在放射学上通常不明显。GPA 患者出现肾肿块虽然极为罕见,但可以识别。在此,我们报告一例 GPA 表现为孤立性肾肿块的罕见病例,并进行文献复习。
一名 75 岁女性因增强 CT 检查发现右肾单发肿块(大小为 4×3.5cm)就诊。无鼻窦炎、鼻炎、咳嗽或肺炎等提示全身 GPA 的病史。由于怀疑为肾细胞癌或恶性淋巴瘤,进行了肾切除术。三个月后,因血清肌酐水平从 54.81μmol/L 升高至 405.76μmol/L,同时 C 反应蛋白水平升高至 159mg/L,她再次入院。抗中性粒细胞胞浆抗体(抗髓过氧化物酶和抗蛋白酶 3)为阴性。孤立性肾肿块的组织学检查显示皮质和髓质直小血管有坏死性肉芽肿性动脉炎,间质纤维化,局灶节段坏死性肾小球肾炎;然而,孤立性肿块以外的区域未观察到血管炎的迹象。因此,该患者被诊断为 GPA。尽管给予泼尼松(30mg/天)治疗,但患者出现少尿,血清肌酐水平升高至 583.44μmol/L,激素治疗开始后 1 个月内需要血液透析。患者成功停用血液透析,21 个月后血清肌酐水平降至 251.06μmol/L。
GPA 应被视为孤立性肾肿块的鉴别诊断之一。此外,伴有 GPA 的孤立性肾肿块患者对激素或免疫抑制治疗可能有良好的反应。