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Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years

INTRODUCTION: Solitary cavernous lymphangioma is very rare disease characterized by abnormally proliferating lymphatic vessels. We report a 49-year-old woman with a cavernous pulmonary lymphangioma showing rapid growth after remaining indolent for 10 years. PRESENTATION OF CASE: Chest computed tomog...

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Autores principales: Shinohara, Shinji, Nakanishi, Ryoichi, Yasuda, Manabu, Tanaka, Fumihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018072/
https://www.ncbi.nlm.nih.gov/pubmed/27614339
http://dx.doi.org/10.1016/j.ijscr.2016.08.033
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author Shinohara, Shinji
Nakanishi, Ryoichi
Yasuda, Manabu
Tanaka, Fumihiro
author_facet Shinohara, Shinji
Nakanishi, Ryoichi
Yasuda, Manabu
Tanaka, Fumihiro
author_sort Shinohara, Shinji
collection PubMed
description INTRODUCTION: Solitary cavernous lymphangioma is very rare disease characterized by abnormally proliferating lymphatic vessels. We report a 49-year-old woman with a cavernous pulmonary lymphangioma showing rapid growth after remaining indolent for 10 years. PRESENTATION OF CASE: Chest computed tomography revealed a solitary, poorly demarcated mass in the left lower lobe; however, the tumour grew in size over the next 6 months. A left lower lobectomy was performed following suspected lung cancer. Histopathological and immunohistochemical analysis of the resected specimens revealed a pulmonary cavernous lymphangioma. DISCUSSION: It is difficult to make an accurate diagnosis of solitary cavernous lymphangioma by imaging findings, therefore a surgical resection is recommended as the diagnostic and therapeutic modality. CONCLUSION: A pulmonary lymphangioma should be included in the differential diagnosis of a rapidly growing tumour.
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spelling pubmed-50180722016-09-16 Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years Shinohara, Shinji Nakanishi, Ryoichi Yasuda, Manabu Tanaka, Fumihiro Int J Surg Case Rep Case Report INTRODUCTION: Solitary cavernous lymphangioma is very rare disease characterized by abnormally proliferating lymphatic vessels. We report a 49-year-old woman with a cavernous pulmonary lymphangioma showing rapid growth after remaining indolent for 10 years. PRESENTATION OF CASE: Chest computed tomography revealed a solitary, poorly demarcated mass in the left lower lobe; however, the tumour grew in size over the next 6 months. A left lower lobectomy was performed following suspected lung cancer. Histopathological and immunohistochemical analysis of the resected specimens revealed a pulmonary cavernous lymphangioma. DISCUSSION: It is difficult to make an accurate diagnosis of solitary cavernous lymphangioma by imaging findings, therefore a surgical resection is recommended as the diagnostic and therapeutic modality. CONCLUSION: A pulmonary lymphangioma should be included in the differential diagnosis of a rapidly growing tumour. Elsevier 2016-08-27 /pmc/articles/PMC5018072/ /pubmed/27614339 http://dx.doi.org/10.1016/j.ijscr.2016.08.033 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Shinohara, Shinji
Nakanishi, Ryoichi
Yasuda, Manabu
Tanaka, Fumihiro
Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
title Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
title_full Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
title_fullStr Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
title_full_unstemmed Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
title_short Rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
title_sort rapid growing pulmonary cavernous lymphangioma after chronic process for ten years
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018072/
https://www.ncbi.nlm.nih.gov/pubmed/27614339
http://dx.doi.org/10.1016/j.ijscr.2016.08.033
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