Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation

Pegvisomant (PEGv) is a growth hormone receptor antagonist approved for the treatment of acromegaly; one of its documented adverse effects is reversible elevation of hepatic enzymes. We report a 39-year-old male acromegalic patient with a pituitary macroadenoma who underwent transsphenoidal surgery....

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Main Authors: Maria Susana Mallea-Gil, Ignacio Bernabeu, Adriana Spiraquis, Alejandra Avangina, Lourdes Loidi, Carolina Ballarino
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2016/2087102
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author Maria Susana Mallea-Gil
Ignacio Bernabeu
Adriana Spiraquis
Alejandra Avangina
Lourdes Loidi
Carolina Ballarino
author_facet Maria Susana Mallea-Gil
Ignacio Bernabeu
Adriana Spiraquis
Alejandra Avangina
Lourdes Loidi
Carolina Ballarino
author_sort Maria Susana Mallea-Gil
collection DOAJ
description Pegvisomant (PEGv) is a growth hormone receptor antagonist approved for the treatment of acromegaly; one of its documented adverse effects is reversible elevation of hepatic enzymes. We report a 39-year-old male acromegalic patient with a pituitary macroadenoma who underwent transsphenoidal surgery. The patient’s condition improved but GH and IGF-I levels did not normalize; as a consequence, we first administered dopamine agonists and then somatostatin receptor ligands (SRLs) with poor response. PEGv 15 mg every other day was added to lanreotide 120 mg monthly. The patient developed a severe hepatitis five months after starting the combination therapy. Elevated ferritin, iron, and transferrin saturation suggested probable hepatitis due to haemochromatosis. We performed a liver biopsy which showed an acute cholestatic hepatitis consistent with toxic etiology. A heterozygous genotype UGT1A1​⁎28 polymorphism associated with Gilbert’s syndrome was also found in this Argentine patient. The predominant clinical presentation resembled an acute cholestatic hepatitis associated with severe hemosiderosis, a different and new pattern of PEGv hepatotoxicity.
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series Case Reports in Endocrinology
spelling doaj-art-0077c11b4c2f47179bbf11ad7ee7a4562025-08-20T02:03:13ZengWileyCase Reports in Endocrinology2090-65012090-651X2016-01-01201610.1155/2016/20871022087102Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 MutationMaria Susana Mallea-Gil0Ignacio Bernabeu1Adriana Spiraquis2Alejandra Avangina3Lourdes Loidi4Carolina Ballarino5Servicio de Endocrinologıa, Hospital Militar Central, 726 Luis María Campos Avenue, 1425 Buenos Aires, ArgentinaEndocrinology Division and Fundacion Publica Galega de Medicina Xenomica (Unidad de Medicina Molecular), Complejo Hospitalario Universitario de Santiago de Compostela, Universidad de Santiago de Compostela, Travesia Choupana s/n, Santiago de Compostela, 15706 La Coruña, SpainServicio de Gastroenterologıa, Hospital Militar Central, 726 Luis María Campos Avenue, 1425 Buenos Aires, ArgentinaDepartamento de Anatomıa Patologica, Hospital de Clínicas, Universidad de Buenos Aires, 2351 Córdoba Avenue, 1120 Buenos Aires, ArgentinaEndocrinology Division and Fundacion Publica Galega de Medicina Xenomica (Unidad de Medicina Molecular), Complejo Hospitalario Universitario de Santiago de Compostela, Universidad de Santiago de Compostela, Travesia Choupana s/n, Santiago de Compostela, 15706 La Coruña, SpainServicio de Endocrinologıa, Hospital Militar Central, 726 Luis María Campos Avenue, 1425 Buenos Aires, ArgentinaPegvisomant (PEGv) is a growth hormone receptor antagonist approved for the treatment of acromegaly; one of its documented adverse effects is reversible elevation of hepatic enzymes. We report a 39-year-old male acromegalic patient with a pituitary macroadenoma who underwent transsphenoidal surgery. The patient’s condition improved but GH and IGF-I levels did not normalize; as a consequence, we first administered dopamine agonists and then somatostatin receptor ligands (SRLs) with poor response. PEGv 15 mg every other day was added to lanreotide 120 mg monthly. The patient developed a severe hepatitis five months after starting the combination therapy. Elevated ferritin, iron, and transferrin saturation suggested probable hepatitis due to haemochromatosis. We performed a liver biopsy which showed an acute cholestatic hepatitis consistent with toxic etiology. A heterozygous genotype UGT1A1​⁎28 polymorphism associated with Gilbert’s syndrome was also found in this Argentine patient. The predominant clinical presentation resembled an acute cholestatic hepatitis associated with severe hemosiderosis, a different and new pattern of PEGv hepatotoxicity.http://dx.doi.org/10.1155/2016/2087102
spellingShingle Maria Susana Mallea-Gil
Ignacio Bernabeu
Adriana Spiraquis
Alejandra Avangina
Lourdes Loidi
Carolina Ballarino
Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation
Case Reports in Endocrinology
title Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation
title_full Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation
title_fullStr Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation
title_full_unstemmed Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation
title_short Pegvisomant-Induced Cholestatic Hepatitis in an Acromegalic Patient with UGT1A1 ​⁎ 28 Mutation
title_sort pegvisomant induced cholestatic hepatitis in an acromegalic patient with ugt1a1 ​  28 mutation
url http://dx.doi.org/10.1155/2016/2087102
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