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Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review

A 65-year-old Italian physician affected by Familial Mediterranean fever (FMF) was hospitalized due to progressive abdominal enlargement, which had begun 6 months before admission. Physical examination revealed ascites and bilateral leg edema. Abdominal CT scan showed ascitic fluid and extensive mul...

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Autores principales: Talerico, Rosa, Cardillo, Carmine, De Vito, Francesco, Schinzari, Francesca, Soldato, Manuel, Giustiniani, Maria Cristina, Verrecchia, Elena, Manna, Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237567/
https://www.ncbi.nlm.nih.gov/pubmed/32477360
http://dx.doi.org/10.3389/fimmu.2020.00889
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author Talerico, Rosa
Cardillo, Carmine
De Vito, Francesco
Schinzari, Francesca
Soldato, Manuel
Giustiniani, Maria Cristina
Verrecchia, Elena
Manna, Raffaele
author_facet Talerico, Rosa
Cardillo, Carmine
De Vito, Francesco
Schinzari, Francesca
Soldato, Manuel
Giustiniani, Maria Cristina
Verrecchia, Elena
Manna, Raffaele
author_sort Talerico, Rosa
collection PubMed
description A 65-year-old Italian physician affected by Familial Mediterranean fever (FMF) was hospitalized due to progressive abdominal enlargement, which had begun 6 months before admission. Physical examination revealed ascites and bilateral leg edema. Abdominal CT scan showed ascitic fluid and extensive multiple peritoneal implants; peritoneal CT-guided biopsy revealed an epithelial-type malignant mesothelioma. The patient's past medical history revealed recurrent episodes of abdominal pain and fever from the age of 2. Clinical diagnosis of FMF was suspected at the age of 25, while genetic analysis, performed at the age of 50, confirmed homozygosity for the M694I mutation in the MEFV gene. Treatment with the first line FMF drug colchicine was started and stopped several times because of worsened leukopenia. The patient in fact had a history of asymptomatic leukopenia/lymphopenia from an early age; the intake of colchicine aggravated his pre-existing problem until the definitive suspension of the drug. As for second-line drugs, canakinumab was first prescribed, but due to prescription issues, it was not possible to be administered. When he was given anakinra, there was a worsening of leukopenia leading to septic fever. Systematic literature review indicates that, in most cases, recurrent peritoneal inflammation results in benign peritoneal fibrosis or less commonly in encapsulating peritonitis. There are only a few reported cases of recurrent peritoneal inflammation progressing from FMF to peritoneal mesothelioma (MST). In such cases, intolerance to colchicine or its erratic intake may lead to long-term recurrent inflammation, which usually precedes the development of the tumor, while pre-existing leukopenia, as in our patient, could also be a factor promoting or accelerating the tumor progression. In conclusion, we suggest that in the presence of intolerance or resistance to colchicine, interleukin (IL)-1 inhibition could suppress peritoneal inflammation and prevent MSTs.
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spelling pubmed-72375672020-05-29 Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review Talerico, Rosa Cardillo, Carmine De Vito, Francesco Schinzari, Francesca Soldato, Manuel Giustiniani, Maria Cristina Verrecchia, Elena Manna, Raffaele Front Immunol Immunology A 65-year-old Italian physician affected by Familial Mediterranean fever (FMF) was hospitalized due to progressive abdominal enlargement, which had begun 6 months before admission. Physical examination revealed ascites and bilateral leg edema. Abdominal CT scan showed ascitic fluid and extensive multiple peritoneal implants; peritoneal CT-guided biopsy revealed an epithelial-type malignant mesothelioma. The patient's past medical history revealed recurrent episodes of abdominal pain and fever from the age of 2. Clinical diagnosis of FMF was suspected at the age of 25, while genetic analysis, performed at the age of 50, confirmed homozygosity for the M694I mutation in the MEFV gene. Treatment with the first line FMF drug colchicine was started and stopped several times because of worsened leukopenia. The patient in fact had a history of asymptomatic leukopenia/lymphopenia from an early age; the intake of colchicine aggravated his pre-existing problem until the definitive suspension of the drug. As for second-line drugs, canakinumab was first prescribed, but due to prescription issues, it was not possible to be administered. When he was given anakinra, there was a worsening of leukopenia leading to septic fever. Systematic literature review indicates that, in most cases, recurrent peritoneal inflammation results in benign peritoneal fibrosis or less commonly in encapsulating peritonitis. There are only a few reported cases of recurrent peritoneal inflammation progressing from FMF to peritoneal mesothelioma (MST). In such cases, intolerance to colchicine or its erratic intake may lead to long-term recurrent inflammation, which usually precedes the development of the tumor, while pre-existing leukopenia, as in our patient, could also be a factor promoting or accelerating the tumor progression. In conclusion, we suggest that in the presence of intolerance or resistance to colchicine, interleukin (IL)-1 inhibition could suppress peritoneal inflammation and prevent MSTs. Frontiers Media S.A. 2020-05-13 /pmc/articles/PMC7237567/ /pubmed/32477360 http://dx.doi.org/10.3389/fimmu.2020.00889 Text en Copyright © 2020 Talerico, Cardillo, De Vito, Schinzari, Soldato, Giustiniani, Verrecchia and Manna. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Talerico, Rosa
Cardillo, Carmine
De Vito, Francesco
Schinzari, Francesca
Soldato, Manuel
Giustiniani, Maria Cristina
Verrecchia, Elena
Manna, Raffaele
Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review
title Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review
title_full Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review
title_fullStr Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review
title_full_unstemmed Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review
title_short Mesothelioma in Familial Mediterranean Fever With Colchicine Intolerance: A Case Report and Literature Review
title_sort mesothelioma in familial mediterranean fever with colchicine intolerance: a case report and literature review
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237567/
https://www.ncbi.nlm.nih.gov/pubmed/32477360
http://dx.doi.org/10.3389/fimmu.2020.00889
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