Minimal change disease induced by tiopronin: a rare case report and a review of the literature

被引:9
|
作者
Zhong, Han [1 ]
Wang, Ling [2 ]
Gu, Zhi-Chun [1 ]
Cui, Min [1 ]
Liu, Xiao-Yan [1 ]
Pang, Xiao-Yun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Pharm, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Nephrol, Shanghai 200127, Peoples R China
关键词
Minimal change disease (MCD); nephrotic syndrome (NS); tiopronin (TP); adverse drug reaction; NEPHROTIC SYNDROME; RHEUMATOID-ARTHRITIS; NEPHROPATHY; RIFAMPICIN; EFFICACY;
D O I
10.21037/atm.2019.07.42
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tiopronin (TP), a glycine derivative with a free thiol, is extensively used for the treatment of cystinuria. Moreover, TP is usually prescribed as hepatoprotective medicine in China. In the present case, a 36-year-old female who presented with foamy urine and general edema was admitted to the hospital. She had been taking TP for six months to treat drug-induced liver injury due to anti-tuberculosis drugs including isoniazid, rifampicin and pyrazinamide. The urine tests at admission revealed nephritic-range proteinuria with a daily urinary protein level of 8,024 mg. Meanwhile, albumin and cholesterol levels were abnormal. The light microscopy was negative and electron microscopy showed foot process effacement. Thus, minimal change disease (MCD) was diagnosed, and TP was consequently discontinued. Finally, the patient accomplished complete remission within five weeks after the cessation of TP without undergoing glucocorticoid therapy. TP was speculated to play an antigenic role in this adverse effect. To date, there are only two similar cases documented in the literature. Herein, we first report a case of a Chinese patient who generated MCD after prolonged TP administration. Clinicians should be wary of the occurrence of MCD due to TP when administering long-term therapy of TP. A weekly urinalysis may be useful for early identification of TP-induced MCD.
引用
收藏
页数:6
相关论文
共 50 条
  • [41] Bilateral Achilles Tendon Ruptures Associated With Ciprofloxacin Use in the Setting of Minimal Change Disease: Case Report and Review of the Literature
    Kawtharani, Firas
    Masrouha, Karim Z.
    Afeiche, Nadim
    JOURNAL OF FOOT & ANKLE SURGERY, 2016, 55 (02): : 276 - 278
  • [42] Relapse of minimal change disease following the third mRNA COVID-19 vaccination: a case report and literature review
    Teragaki, Mariko
    Tanaka, Mari
    Yamamoto, Hiroko
    Watanabe, Tomoka
    Takeoka, Jun
    Fukumi, Awaisshafig
    Maeda, Kotaro
    Takami, Yohtaro
    Saita, Hirona
    Iwanari, Sachio
    Ikeda, Masaki
    Takeoka, Hiroya
    CEN CASE REPORTS, 2024, 13 (01) : 53 - 58
  • [43] Primary Sjogren's syndrome with minimal change disease: case series and literature review
    Lang, J.
    Shi, X.
    Ma, Y.
    Zou, L.
    Fei, Y.
    Chen, L.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2021, 39 (06) : S226 - S227
  • [44] Celecoxib-induced drug fever: A rare case report and literature review
    Xiao, Jing
    Jia, Su-Jie
    Wu, Cui-Fang
    JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, 2022, 47 (03) : 402 - 406
  • [45] Rare skin adverse reactions induced by osimertinib: a case report and literature review
    Zhang, Ye
    Ling, Mingzhu
    Wang, Min
    Chen, Ye
    Zhang, Liting
    FRONTIERS IN ONCOLOGY, 2025, 15
  • [46] MINIMAL CHANGE DISEASE (MCD) IN PATIENT OF ULCERATIVE COLITIS (UC), ADVERSE REACTION TO BALSALAZIDE OR DISEASE ASSOCIATION? LITERATURE REVIEW & CASE REPORT
    Gera, Manish
    Jeevan, R.
    Dhar, S.
    Gera, P. S.
    Phillips, C. L.
    AMERICAN JOURNAL OF KIDNEY DISEASES, 2010, 55 (04) : A57 - A57
  • [47] Rare Finding of Leptomeningeal Disease in Colorectal Carcinoma: A Case Report and Review of the Literature
    Aronson, Kerri
    Cohen, Michelle
    Kumta, Nikhil
    Wan, David
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2013, 108 : S398 - S398
  • [48] Aphasia as a rare presentation of monosymptomatic demyelinating disease: case report and review of the literature
    L. Di Majo
    M. Bisceglia
    R. Lanzillo
    V. D'Angelo
    L. Gorgoglione
    L. Chiacchio
    G. Orefice
    Neurological Sciences, 2002, 23 : 79 - 82
  • [49] Erdheim-Chester disease: a rare histiocytosis (case report and review of the literature)
    El Mehdi, Mahtat
    Regragui, Safae
    Eddou, Hicham
    Jennane, Selim
    El Maaroufi, Hicham
    Doghmi, Kamal
    Mikdame, Mohamed
    PAN AFRICAN MEDICAL JOURNAL, 2018, 29
  • [50] Rosai-Dorfman disease of the maxilla: A rare case report and literature review
    Nagai, Takahiro
    Yamazaki, Manabu
    Nishikawa, Atsushi
    Kodama, Yasumitsu
    Nishiyama, Hideyoshi
    Hayashi, Takafumi
    Tanuma, Jun-ichi
    Takagi, Ritsuo
    Tomihara, Kei
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY MEDICINE AND PATHOLOGY, 2022, 34 (05) : 665 - 671