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Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome

Cytokine storm caused by the overproduction of inflammatory interleukin (IL)-6 plays a central role in the development of acute inflammation. The extremely rare disease, TAFRO syndrome, progresses quickly. Renal dysfunction, fever, reticulin fibrosis, anasarca, thrombocytopenia, and organomegaly wit...

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Autores principales: Shimada, Yoshitaka, Nagaba, Yasushi, Fujino, Mako, Okawa, Hiroyuki, Ehara, Kaori, Shishido, Eri, Okada, Shinya, Yokomori, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512824/
https://www.ncbi.nlm.nih.gov/pubmed/37746092
http://dx.doi.org/10.3389/fmed.2023.1137899
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author Shimada, Yoshitaka
Nagaba, Yasushi
Fujino, Mako
Okawa, Hiroyuki
Ehara, Kaori
Shishido, Eri
Okada, Shinya
Yokomori, Hiroaki
author_facet Shimada, Yoshitaka
Nagaba, Yasushi
Fujino, Mako
Okawa, Hiroyuki
Ehara, Kaori
Shishido, Eri
Okada, Shinya
Yokomori, Hiroaki
author_sort Shimada, Yoshitaka
collection PubMed
description Cytokine storm caused by the overproduction of inflammatory interleukin (IL)-6 plays a central role in the development of acute inflammation. The extremely rare disease, TAFRO syndrome, progresses quickly. Renal dysfunction, fever, reticulin fibrosis, anasarca, thrombocytopenia, and organomegaly with pathological findings such as idiopathic multicentric Castleman disease are all characteristics of TAFRO syndrome. Interstitial pneumonia (IP), which is not characteristic of this disease, is probably a complication of the inflammatory process. An 88-year-old man presented with a 3-day history of fever, dry cough, and progressive dyspnea. After he was first treated with antibiotics, he was transferred to our hospital because he showed no improvement. Data showed hemoglobin Hb 90.00 (SI) (9.0 g/dL); leukocyte count WBC 23 × 10(9)/L (SI) [23,000/μL (neutrophils 87.5%, lymphocytes 2.5%, blast cells 0%)]; hemoglobin 90 g/L (9.0 g/dL); platelet count 101.00 × 10(9)/L (10 100/μL); lactate dehydrogenase 4.78 μkat/L (286 U/L); serum albumin 25.00 g/L (2.5 g/dL); blood urea nitrogen 18.17 μmol/L (50.9 mg/dL); creatinine 285.53 μmol/L (3.23 mg/dL); C-reactive protein 161.50 mg/L (16.15 mg/dL); IL-61830 pg/mL; and surfactant protein D level 26.6 ng/mL. Findings from computed tomography indicated increased ground-glass opacities without traction bronchiectasis consistent with acute IP. The diagnosis was leukocytosis and progressive kidney injury. After bone marrow aspiration caused by persistent pancytopenia, mild reticulin fibrosis was identified. Because of the high IL-6 concentration, which revealed small atrophic follicles with regressed germinal centers surrounded by several lymphocytes, right inguinal lymph node biopsy was performed. Two minor and three major criteria led to diagnosis of TAFRO syndrome. Administrations of antibiotic therapy and methylprednisolone pulse therapy were ineffective. After rapid progress of respiratory failure, the patient died on day 30 of hospitalization. Autopsy of lung tissues showed diffuse alveolar damage with hyaline membranes. Based on these findings, we diagnosed acute exacerbation of IP associated with TAFRO syndrome due to IL-6 overproduction-associated cytokine storm.
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spelling pubmed-105128242023-09-22 Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome Shimada, Yoshitaka Nagaba, Yasushi Fujino, Mako Okawa, Hiroyuki Ehara, Kaori Shishido, Eri Okada, Shinya Yokomori, Hiroaki Front Med (Lausanne) Medicine Cytokine storm caused by the overproduction of inflammatory interleukin (IL)-6 plays a central role in the development of acute inflammation. The extremely rare disease, TAFRO syndrome, progresses quickly. Renal dysfunction, fever, reticulin fibrosis, anasarca, thrombocytopenia, and organomegaly with pathological findings such as idiopathic multicentric Castleman disease are all characteristics of TAFRO syndrome. Interstitial pneumonia (IP), which is not characteristic of this disease, is probably a complication of the inflammatory process. An 88-year-old man presented with a 3-day history of fever, dry cough, and progressive dyspnea. After he was first treated with antibiotics, he was transferred to our hospital because he showed no improvement. Data showed hemoglobin Hb 90.00 (SI) (9.0 g/dL); leukocyte count WBC 23 × 10(9)/L (SI) [23,000/μL (neutrophils 87.5%, lymphocytes 2.5%, blast cells 0%)]; hemoglobin 90 g/L (9.0 g/dL); platelet count 101.00 × 10(9)/L (10 100/μL); lactate dehydrogenase 4.78 μkat/L (286 U/L); serum albumin 25.00 g/L (2.5 g/dL); blood urea nitrogen 18.17 μmol/L (50.9 mg/dL); creatinine 285.53 μmol/L (3.23 mg/dL); C-reactive protein 161.50 mg/L (16.15 mg/dL); IL-61830 pg/mL; and surfactant protein D level 26.6 ng/mL. Findings from computed tomography indicated increased ground-glass opacities without traction bronchiectasis consistent with acute IP. The diagnosis was leukocytosis and progressive kidney injury. After bone marrow aspiration caused by persistent pancytopenia, mild reticulin fibrosis was identified. Because of the high IL-6 concentration, which revealed small atrophic follicles with regressed germinal centers surrounded by several lymphocytes, right inguinal lymph node biopsy was performed. Two minor and three major criteria led to diagnosis of TAFRO syndrome. Administrations of antibiotic therapy and methylprednisolone pulse therapy were ineffective. After rapid progress of respiratory failure, the patient died on day 30 of hospitalization. Autopsy of lung tissues showed diffuse alveolar damage with hyaline membranes. Based on these findings, we diagnosed acute exacerbation of IP associated with TAFRO syndrome due to IL-6 overproduction-associated cytokine storm. Frontiers Media S.A. 2023-09-07 /pmc/articles/PMC10512824/ /pubmed/37746092 http://dx.doi.org/10.3389/fmed.2023.1137899 Text en Copyright © 2023 Shimada, Nagaba, Fujino, Okawa, Ehara, Shishido, Okada and Yokomori. https://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 Medicine
Shimada, Yoshitaka
Nagaba, Yasushi
Fujino, Mako
Okawa, Hiroyuki
Ehara, Kaori
Shishido, Eri
Okada, Shinya
Yokomori, Hiroaki
Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome
title Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome
title_full Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome
title_fullStr Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome
title_full_unstemmed Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome
title_short Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome
title_sort case report: a case of acute exacerbation of interstitial pneumonia associated with tafro syndrome
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512824/
https://www.ncbi.nlm.nih.gov/pubmed/37746092
http://dx.doi.org/10.3389/fmed.2023.1137899
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