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CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS
A previously healthy, 52-year-old woman presented with a nine months history of low fever and weight loss (> 30 kg). Physical examination disclosed generalized lymphadenopathy, skin lesions, abdominal distension, mild tachypnea and a left breast mass. Laboratory tests showed anemia; (prerenal) ki...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Instituto de Medicina Tropical
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964326/ https://www.ncbi.nlm.nih.gov/pubmed/27410917 http://dx.doi.org/10.1590/S1678-9946201658057 |
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author | FERNANDES, Flávia Fonseca ALVES, Victor Oliveira SÁNCHEZ, Tarquino Erastides Gavilanes de PAULA, Wagner Diniz SANTANA, Alfredo Nicodemos Cruz |
author_facet | FERNANDES, Flávia Fonseca ALVES, Victor Oliveira SÁNCHEZ, Tarquino Erastides Gavilanes de PAULA, Wagner Diniz SANTANA, Alfredo Nicodemos Cruz |
author_sort | FERNANDES, Flávia Fonseca |
collection | PubMed |
description | A previously healthy, 52-year-old woman presented with a nine months history of low fever and weight loss (> 30 kg). Physical examination disclosed generalized lymphadenopathy, skin lesions, abdominal distension, mild tachypnea and a left breast mass. Laboratory tests showed anemia; (prerenal) kidney injury, low serum albumin level; and negative serology for HIV and viral hepatitis. Computed tomography (neck/chest/abdomen) showed generalized lymph node enlargement, splenomegaly, pleural effusion and ascites. We performed thoracocentesis and paracentesis, and the findings were consistent with chylothorax and chylous ascites (with no neoplastic cells). Biopsies of the breast mass, skin and lymph nodes were performed and all of them showed large round yeast cells with multiple narrow-based budding daughter cells, characteristic of Paracoccidioides brasiliensis. Consequently, paracoccidioidomycosis was diagnosed, and liposomal amphotericin B was prescribed, as well as a high protein and low fat diet (supplemented with medium chain triglycerides). Even so, her clinical status worsened, requiring renal replacement therapy. She evolved with pneumonia, septic shock and respiratory failure and subsequently died. To our knowledge, this is the first description of a case with chylothorax and breast mass due to paracoccidioidomycosis. Additionally, we discuss: 1- the importance of the inclusion of this mycosis in the differential diagnosis of chylothorax and breast mass (breast cancer), especially in endemic areas; and 2- the possible mechanism involved in the development of chylous effusions. |
format | Online Article Text |
id | pubmed-4964326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Instituto de Medicina Tropical |
record_format | MEDLINE/PubMed |
spelling | pubmed-49643262016-08-08 CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS FERNANDES, Flávia Fonseca ALVES, Victor Oliveira SÁNCHEZ, Tarquino Erastides Gavilanes de PAULA, Wagner Diniz SANTANA, Alfredo Nicodemos Cruz Rev Inst Med Trop Sao Paulo Case Report A previously healthy, 52-year-old woman presented with a nine months history of low fever and weight loss (> 30 kg). Physical examination disclosed generalized lymphadenopathy, skin lesions, abdominal distension, mild tachypnea and a left breast mass. Laboratory tests showed anemia; (prerenal) kidney injury, low serum albumin level; and negative serology for HIV and viral hepatitis. Computed tomography (neck/chest/abdomen) showed generalized lymph node enlargement, splenomegaly, pleural effusion and ascites. We performed thoracocentesis and paracentesis, and the findings were consistent with chylothorax and chylous ascites (with no neoplastic cells). Biopsies of the breast mass, skin and lymph nodes were performed and all of them showed large round yeast cells with multiple narrow-based budding daughter cells, characteristic of Paracoccidioides brasiliensis. Consequently, paracoccidioidomycosis was diagnosed, and liposomal amphotericin B was prescribed, as well as a high protein and low fat diet (supplemented with medium chain triglycerides). Even so, her clinical status worsened, requiring renal replacement therapy. She evolved with pneumonia, septic shock and respiratory failure and subsequently died. To our knowledge, this is the first description of a case with chylothorax and breast mass due to paracoccidioidomycosis. Additionally, we discuss: 1- the importance of the inclusion of this mycosis in the differential diagnosis of chylothorax and breast mass (breast cancer), especially in endemic areas; and 2- the possible mechanism involved in the development of chylous effusions. Instituto de Medicina Tropical 2016-07-11 /pmc/articles/PMC4964326/ /pubmed/27410917 http://dx.doi.org/10.1590/S1678-9946201658057 Text en http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License |
spellingShingle | Case Report FERNANDES, Flávia Fonseca ALVES, Victor Oliveira SÁNCHEZ, Tarquino Erastides Gavilanes de PAULA, Wagner Diniz SANTANA, Alfredo Nicodemos Cruz CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS |
title | CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS |
title_full | CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS |
title_fullStr | CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS |
title_full_unstemmed | CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS |
title_short | CHYLOTHORAX IN PARACOCCIDIOIDOMYCOSIS |
title_sort | chylothorax in paracoccidioidomycosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964326/ https://www.ncbi.nlm.nih.gov/pubmed/27410917 http://dx.doi.org/10.1590/S1678-9946201658057 |
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