Rapidly Progressive Renal Failure in Young Adult: An Atypical Presentation of Multiple Myeloma - A Case Report

Himanish Goswami, Tonmoy Das, Mitul Bora, Sweety Kakoti, Tanurekha Hazarika, Dhruvajyoti Choudhury, Pranab Medhi, Zenila Bordoloi, Madhurima Dutta, S. Choudhury
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Abstract

Patients frequently present with renal impairment that does not fit the criteria for acute kidney injury or chronic kidney disease. This condition, known as rapidly progressive renal failure (RPRF), encompasses a diverse range of clinical syndromes characterized by the progressive renal impairment over days to weeks. We present a case of a 37-year-old male with a short history of uremic symptoms and decreased urine output with no significant history or examination findings except pallor. The patient had a creatinine of 1.6 mg/dL in April 2022, rising to 4.4 mg/dL, then 11.6 mg/dL during May, 17.6 mg/dL in June, presented to us with a creatinine of 24.6 mg/dL, with normal kidney size and corticomedullary differentiation (CMD). Beta-2-microglobulin was elevated, and renal biopsy showed features suggestive of multiple myeloma (MM). Atypical appearing tubular casts showing 3+ patternless staining for kappa light chains and negativity for lambda light chains were observed. The patient was started on chemotherapy for MM, and renal function was gradually improving. Renal failure as the sole presentation of MM is rare, especially in young adults. This case emphasizes an atypical RPRF, particularly given the patient’s young age.
年轻成人快速进展性肾衰竭:多发性骨髓瘤的非典型表现--病例报告
患者经常会出现肾功能损害,但却不符合急性肾损伤或慢性肾病的标准。这种情况被称为快速进展性肾功能衰竭(RPRF),包括多种临床综合征,其特点是数天至数周内肾功能逐渐受损。我们介绍了一例 37 岁男性患者的病例,该患者有尿毒症症状和尿量减少的短暂病史,除面色苍白外无其他明显病史或检查结果。患者 2022 年 4 月的血肌酐为 1.6 毫克/分升,随后升至 4.4 毫克/分升,5 月为 11.6 毫克/分升,6 月为 17.6 毫克/分升,就诊时血肌酐为 24.6 毫克/分升,肾脏大小正常,皮质髓质分化(CMD)。β-2-微球蛋白升高,肾活检显示多发性骨髓瘤(MM)的特征。观察到肾小管出现非典型铸型,卡帕轻链呈3+无模式染色,λ轻链呈阴性。患者开始接受 MM 化疗,肾功能逐渐好转。肾功能衰竭作为MM的唯一表现并不多见,尤其是在年轻人中。本病例强调的是一种非典型的肾功能衰竭,尤其是考虑到患者的年轻。
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