Acute kidney injury secondary to thrombotic microangiopathy associated with idiopathic hypereosinophilic syndrome: a case report and review of the literature

被引:2
作者
Curras-Martin, Diana [1 ]
Patel, Swapnil [1 ]
Qaisar, Huzaif [1 ]
Mehandru, Sushil K. [1 ]
Masud, Avais [1 ]
Hossain, Mohammad A. [1 ]
Lamba, Gurpreet S. [1 ]
Dounis, Harry [1 ]
Levitt, Michael [1 ]
Asif, Arif [1 ]
机构
[1] Jersey Shore Univ, Med Ctr, Hackensack Meridian Hlth, Dept Med,Internal Med Residency Program, Hackensack, NJ 07753 USA
关键词
Idiopathic hypereosinophilic syndrome; Eosinophilic cytotoxicity; Thrombotic microangiopathy; RENAL INVOLVEMENT; PATIENT;
D O I
10.1186/s13256-019-2187-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Renal involvement in idiopathic hypereosinophilic syndrome is uncommon. The mechanism of kidney damage can be explained as occurring via two distinct pathways: (1) thromboembolic ischemic changes secondary to endocardial disruption mediated by eosinophilic cytotoxicity to the myocardium and (2) direct eosinophilic cytotoxic effect to the kidney. Case presentation We present a case of a 63-year-old Caucasian man who presented to our hospital with 2 weeks of progressively generalized weakness. He was diagnosed with idiopathic hypereosinophilic syndrome with multiorgan involvement and acute kidney injury with biopsy-proven thrombotic microangiopathy. Full remission was achieved after 8 weeks of corticosteroid therapy. Conclusion Further studies are needed to investigate if age and absence of frank thrombocytopenia can serve as a prognostic feature of idiopathic hypereosinophilic syndrome, as seen in this case.
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共 25 条
  • [1] Mechanisms of eosinophilia in the pathogenesis of hypereosinophilic disorders
    Ackerman, Steven J.
    Bochner, Bruce S.
    [J]. IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2007, 27 (03) : 357 - +
  • [2] Atypical hemolytic uremic syndrome in the setting of complement-amplifying conditions: case reports and a review of the evidence for treatment with eculizumab
    Asif, Arif
    Nayer, Ali
    Haas, Christian S.
    [J]. JOURNAL OF NEPHROLOGY, 2017, 30 (03) : 347 - 362
  • [3] Bulucu F, 2002, CLIN NEPHROL, V57, P171
  • [4] Immunotactoid glomerulopathy associated with idiopathic hypereosinophilic syndrome
    Choi, YJ
    Lee, JD
    Yang, KH
    Woo, JY
    Kim, BK
    Bang, BK
    Shim, SI
    [J]. AMERICAN JOURNAL OF NEPHROLOGY, 1998, 18 (04) : 337 - 343
  • [5] A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
    Cools, J
    DeAngelo, DJ
    Gotlib, J
    Stover, EH
    Legare, RD
    Cortes, J
    Kutok, J
    Clark, J
    Galinsky, I
    Griffin, JD
    Cross, NCP
    Tefferi, A
    Malone, J
    Alam, R
    Schrier, SL
    Schmid, J
    Rose, M
    Vandenberghe, P
    Verhoef, G
    Boogaerts, M
    Wlodarska, I
    Kantarjian, H
    Marynen, P
    Coutre, SE
    Stone, R
    Gilliland, DG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (13) : 1201 - 1214
  • [6] Incidence of myeloproliferative hypereosinophilic syndrome in the United States and an estimate of all hypereosinophilic syndrome incidence
    Crane, Martin M.
    Chang, Cindy Ma
    Kobayashi, Monica G.
    Weller, Peter F.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 126 (01) : 179 - 181
  • [7] The potential role of complements in cocaine-induced thrombotic microangiopathy
    Dejman, Adriana
    Alavi, Seyed Navid
    Thomas, David B.
    Stefanovic, Alexandra
    Asif, Arif
    Nayer, Ali
    [J]. CLINICAL KIDNEY JOURNAL, 2018, 11 (01) : 26 - 28
  • [8] Frigui M, 2010, SAUDI J KIDNEY DIS T, V21, P320
  • [9] Garella G, 1990, Minerva Urol Nefrol, V42, P135
  • [10] World Health Organization-defined eosinophilic disorders: 2017 update on diagnosis, risk stratification, and management
    Gotlib, Jason
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2017, 92 (11) : 1243 - 1259