Cargando…
Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report
BACKGROUND: Splenosis is the heterotopic autotransplantation of splenic tissue after severe splenic trauma and/or splenectomy. The epidemiology is elusive, but splenosis is frequently misdiagnosed as malignant tumors of gastrointestinal, gynecological, or hematological origin before the correct diag...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857824/ https://www.ncbi.nlm.nih.gov/pubmed/35180884 http://dx.doi.org/10.1186/s13256-022-03288-9 |
_version_ | 1784654120409366528 |
---|---|
author | Föh, Bandik Sieren, Malte Maria Both, Marcus Seeger, Marcus Günther, Rainer |
author_facet | Föh, Bandik Sieren, Malte Maria Both, Marcus Seeger, Marcus Günther, Rainer |
author_sort | Föh, Bandik |
collection | PubMed |
description | BACKGROUND: Splenosis is the heterotopic autotransplantation of splenic tissue after severe splenic trauma and/or splenectomy. The epidemiology is elusive, but splenosis is frequently misdiagnosed as malignant tumors of gastrointestinal, gynecological, or hematological origin before the correct diagnosis is ultimately found. We herein report a rare case of combined, extensive intraabdominal and intrathoracic splenosis initially presenting as pleural mesothelioma. CASE PRESENTATION: A 63-year-old Caucasian male presented with dyspnea and recurring thoracic pain. Initial X-ray and computed tomography scans showed disseminated intrathoracic and intraabdominal lesions. Consequently, thoracoabdominal mesothelioma or a polytopically metastasized cancer of unknown origin was suspected. A thorough examination of the patient’s medical history and contrast-enhanced ultrasound by a skilled examiner revealed the diagnosis of extensive abdominal and thoracic splenosis as a consequence of an abdominal gunshot wound with a ruptured diaphragm several decades earlier. Timely diagnosis by noninvasive measures prevented the patient from potential complications of harmful diagnostic procedures, including nuclear imaging and biopsies. The patient is currently treated for hepatitis C and chronic obstructive lung disease, whereas no specific treatment for splenosis is required. CONCLUSIONS: We present a case of rare intrathoracic and intraperitoneal splenosis mimicking mesothelioma. Contrast-enhanced ultrasound and thorough patient history were used for diagnosis and prevented this patient from having to undergo potentially harmful diagnostics. Splenosis can occur after splenic trauma and, consequently, needs to be considered as a rare differential diagnosis to malignant tumors of various origins when a matching patient history is obtained. |
format | Online Article Text |
id | pubmed-8857824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88578242022-02-23 Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report Föh, Bandik Sieren, Malte Maria Both, Marcus Seeger, Marcus Günther, Rainer J Med Case Rep Case Report BACKGROUND: Splenosis is the heterotopic autotransplantation of splenic tissue after severe splenic trauma and/or splenectomy. The epidemiology is elusive, but splenosis is frequently misdiagnosed as malignant tumors of gastrointestinal, gynecological, or hematological origin before the correct diagnosis is ultimately found. We herein report a rare case of combined, extensive intraabdominal and intrathoracic splenosis initially presenting as pleural mesothelioma. CASE PRESENTATION: A 63-year-old Caucasian male presented with dyspnea and recurring thoracic pain. Initial X-ray and computed tomography scans showed disseminated intrathoracic and intraabdominal lesions. Consequently, thoracoabdominal mesothelioma or a polytopically metastasized cancer of unknown origin was suspected. A thorough examination of the patient’s medical history and contrast-enhanced ultrasound by a skilled examiner revealed the diagnosis of extensive abdominal and thoracic splenosis as a consequence of an abdominal gunshot wound with a ruptured diaphragm several decades earlier. Timely diagnosis by noninvasive measures prevented the patient from potential complications of harmful diagnostic procedures, including nuclear imaging and biopsies. The patient is currently treated for hepatitis C and chronic obstructive lung disease, whereas no specific treatment for splenosis is required. CONCLUSIONS: We present a case of rare intrathoracic and intraperitoneal splenosis mimicking mesothelioma. Contrast-enhanced ultrasound and thorough patient history were used for diagnosis and prevented this patient from having to undergo potentially harmful diagnostics. Splenosis can occur after splenic trauma and, consequently, needs to be considered as a rare differential diagnosis to malignant tumors of various origins when a matching patient history is obtained. BioMed Central 2022-02-19 /pmc/articles/PMC8857824/ /pubmed/35180884 http://dx.doi.org/10.1186/s13256-022-03288-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Föh, Bandik Sieren, Malte Maria Both, Marcus Seeger, Marcus Günther, Rainer Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
title | Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
title_full | Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
title_fullStr | Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
title_full_unstemmed | Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
title_short | Extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
title_sort | extensive intrathoracic and intraperitoneal splenosis mimicking mesothelioma: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857824/ https://www.ncbi.nlm.nih.gov/pubmed/35180884 http://dx.doi.org/10.1186/s13256-022-03288-9 |
work_keys_str_mv | AT fohbandik extensiveintrathoracicandintraperitonealsplenosismimickingmesotheliomaacasereport AT sierenmaltemaria extensiveintrathoracicandintraperitonealsplenosismimickingmesotheliomaacasereport AT bothmarcus extensiveintrathoracicandintraperitonealsplenosismimickingmesotheliomaacasereport AT seegermarcus extensiveintrathoracicandintraperitonealsplenosismimickingmesotheliomaacasereport AT guntherrainer extensiveintrathoracicandintraperitonealsplenosismimickingmesotheliomaacasereport |