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Khelifi D, Nacef IB, Rojbi I, et al. Cholestase anictérique: une manifestation hépatique rare d’hyperthyroïdie. [Anicteric cholestasis: a rare hepatic dysfunction caused by hyperthyroidism]. Pan Afr Med J. 2019;34:215doi: 10.11604/pamj.2019.34.215.19988.
Khelifi, D., Nacef, I. B., Rojbi, I., Mchirgui, N., & Khiari, K. (2019). Cholestase anictérique: une manifestation hépatique rare d’hyperthyroïdie. [Anicteric cholestasis: a rare hepatic dysfunction caused by hyperthyroidism]. The Pan African medical journal, 34215. https://doi.org/10.11604/pamj.2019.34.215.19988
Khelifi, Dayssem, et al. "Cholestase anictérique: une manifestation hépatique rare d’hyperthyroïdie." [Anicteric cholestasis: a rare hepatic dysfunction caused by hyperthyroidism]. The Pan African medical journal vol. 34 (2019): 215. doi: https://doi.org/10.11604/pamj.2019.34.215.19988
Khelifi D, Nacef IB, Rojbi I, Mchirgui N, Khiari K. Cholestase anictérique: une manifestation hépatique rare d’hyperthyroïdie. [Anicteric cholestasis: a rare hepatic dysfunction caused by hyperthyroidism]. Pan Afr Med J. 2019 Dec 30;34:215. doi: 10.11604/pamj.2019.34.215.19988. eCollection 2019. French. PMID: 32180887; PMCID: PMC7060941.
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Pan Afr Med J. 2019 Dec 30;34:215. doi: 10.11604/pamj.2019.34.215.19988. eCollection 2019.

[Anicteric cholestasis: a rare hepatic dysfunction caused by hyperthyroidism].

The Pan African medical journal

[Article in French]
Dayssem Khelifi, Ibtissem Ben Nacef, Imen Rojbi, Nadia Mchirgui, Karima Khiari

Affiliations

  1. Université de Tunis El Manar, Faculté de Médecine de Tunis, Service d'Endocrinologie-Diabétologie, Hôpital Charles Nicolle, Tunis, Tunisie.

PMID: 32180887 PMCID: PMC7060941 DOI: 10.11604/pamj.2019.34.215.19988

Abstract

Clinical manifestations and visceral involvements described in patients with thyroid disease are many and varied. However, cases of patients with hepatic manifestations have been rarely reported in the literature. We here report the case of a 50 year old patient diagnosed with Graves' disease without a goiter or ocular manifestations. Follow-up laboratory testing led to the detection of anicteric cholestasis. Investigations of the potential causes were negative and given the normalization of the liver parameters after appropriate treatment of hyperthyroidism, the diagnosis of hepatic involvement secondary to Graves' disease was retained. The purpose of this study was to report a new case of rare hepatic manifestation (cholestasis anictérique) in a patient with hyperthyroidism: Graves' disease.

© Dayssem Khelifi et al.

Keywords: Anicteric cholestasis; Graves’ disease; hyperthyroidism

Conflict of interest statement

Les auteurs ne déclarent aucun conflit d'intérêts.

References

  1. J Med Case Rep. 2008 Apr 21;2:116 - PubMed
  2. Ann Intern Med. 1993 Mar 15;118(6):424-8 - PubMed
  3. Case Rep Med. 2014;2014:790458 - PubMed
  4. Pan Afr Med J. 2018 Oct 02;31:72 - PubMed
  5. Mil Med. 1978 Aug;143(8):548-51 - PubMed
  6. Am J Gastroenterol. 1994 Jul;89(7):1071-6 - PubMed

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