Onozawa Yuna, Koizumi Masahiro, Nakagawa Yosuke, Ogura Go, Oki Masayuki, Wada Takehiko, Fukagawa Masafumi
Division of Nephrology, Endocrinology, and Metabolism, Tokai University School of Medicine, 143 Shimokasuya, Isehara City, Kanagawa, 259-1193, Japan.
Division of Pathology, Tokai University School of Medicine, Isehara City, Kanagawa, Japan.
CEN Case Rep. 2025 Apr;14(2):171-177. doi: 10.1007/s13730-024-00925-8. Epub 2024 Aug 20.
Pauci-immune crescentic glomerulonephritis (PICGN) is one of the pathologies causing rapidly progressive glomerulonephritis, often associated with anti-neutrophil cytoplasmic antibody (ANCA); however, in 10-30% of cases, ANCAs are negative. While a relatively large number of cases of ANCA-positive PICGN complicated with malignancy have been previously reported, the number of cases of ANCA-negative PICGN with malignancy is limited. The prognosis for such cases was poor, and many patients died within a relatively short period. Here, we report the case of ANCA-negative PICGN complicated with malignancy successfully treated by corticosteroid and radiation therapy. A 63-year-old Japanese man was admitted to our hospital due to spiking fevers in the previous 3 months. Based on the findings of imaging and pathological tests, he was diagnosed with locally advanced lung adenocarcinoma with mediastinal involvement. After admission, his renal function rapidly deteriorated, and urinalysis showed heavy proteinuria. In serological tests, serology for autoantibodies, including ANCAs, was negative. The kidney biopsy revealed PICGN with prominent endocapillary proliferation. We administered corticosteroid therapy for glomerulonephritis and subsequent radiation therapy for lung carcinoma, both of which were effective. He has been alive without progression of malignancy or kidney disease for 5 years after discharge. In patients with malignancy presenting with acute deterioration of kidney function, although infrequent, one of the conceivable pathological conditions to consider is ANCA-negative PICGN associated with malignancy. In such cases, even with negative antibodies such as ANCA, pathological examination is warranted, and a combination of anti-tumor therapy and immunosuppressive therapy is expected to be effective.
寡免疫性新月体性肾小球肾炎(PICGN)是导致快速进展性肾小球肾炎的病理类型之一,常与抗中性粒细胞胞浆抗体(ANCA)相关;然而,在10%-30%的病例中,ANCA为阴性。虽然先前已报道了相对较多例ANCA阳性的PICGN合并恶性肿瘤的病例,但ANCA阴性的PICGN合并恶性肿瘤的病例数量有限。这类病例的预后较差,许多患者在相对较短的时间内死亡。在此,我们报告1例经皮质类固醇和放射治疗成功治愈的ANCA阴性PICGN合并恶性肿瘤的病例。一名63岁的日本男性因前3个月反复发热入院。根据影像学和病理检查结果,他被诊断为局部晚期肺腺癌伴纵隔受累。入院后,他的肾功能迅速恶化,尿液分析显示大量蛋白尿。血清学检查中,包括ANCA在内的自身抗体血清学检查均为阴性。肾活检显示为具有显著毛细血管内增生的PICGN。我们对肾小球肾炎给予皮质类固醇治疗,随后对肺癌进行放射治疗,二者均有效。出院后5年,他一直存活,恶性肿瘤和肾脏疾病均无进展。对于出现肾功能急性恶化的恶性肿瘤患者,尽管这种情况不常见,但一种可考虑的病理状况是与恶性肿瘤相关的ANCA阴性PICGN。在这类病例中,即使抗体如ANCA为阴性,也有必要进行病理检查,并且抗肿瘤治疗和免疫抑制治疗联合应用有望有效。