Hepatocellular Cholestasis and Pruritus: Beyond Clinical Treatment

Ml, Zanotelli; Feier, Flávia Heinz; Mazzini, Guilherme S.; Wietzycoski, Cácio Ricardo; Vieira, S; Goldani, Helena Ayako Sueno

doi:10.1055/s-0031-1275725

Cited by 2 publications

(1 citation statement)

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“…PFIC type III might appear later in life, and patients have troubled hepatocellular phospholipid export. This type has been linked with suicide [ 1 , 3 , 10 ].…”

Section: Introductionmentioning

confidence: 99%

Dental management of a pediatric patient with progressive familial intrahepatic cholestasis having dental anomalies: a case report and brief review of the literature

et al. 2023

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Background Progressive familial intrahepatic cholestasis is a heterogeneous group of disorders, leading to intrahepatic cholestasis, with the possibility of chronic liver failure and biliary cirrhosis. Oligodontia is either the manifestation of a specific syndrome or is non-syndromic. To the best of our knowledge, this is the first case report of type 3 progressive familial intrahepatic cholestasis and concurrent oligodontia, craniosynostosis, dens in dente, taurodontism, and delayed permanent dentition in the medical and dental literature. Case presentation We present the dental and medical histories and comprehensive dental management of a girl with type 3 progressive familial intrahepatic cholestasis and several dental anomalies, who was referred to a dental clinic due to severe dental caries and pain. Conclusion Our findings suggest that PFIC with manifestations as oligodontia, craniosynostosis, dens in dente, taurodontism, and delayed permanent dentition, might indicate an unknown syndrome; otherwise, the craniofacial anomalies are the manifestations of an independent disease coinciding with PFIC. Moreover, our case is a good example of the importance of timely medical and dental care in confining further health-related complications. The patient was able to ingest without any pain or discomfort after receiving proper dental management.

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“…PFIC type III might appear later in life, and patients have troubled hepatocellular phospholipid export. This type has been linked with suicide [ 1 , 3 , 10 ].…”

Section: Introductionmentioning

confidence: 99%