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Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review
INTRODUCTION: Solitary pulmonary capillary hemangioma (SPCH) is a rare benign lung tumor that clinically resembles early lung cancer and precancerous pulmonary lesions that present with similar imaging manifestations. PRESENTATION OF CASE: The patient was a 54-year-old Japanese man who was referred...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490444/ https://www.ncbi.nlm.nih.gov/pubmed/32916614 http://dx.doi.org/10.1016/j.ijscr.2020.08.020 |
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author | Komatsu, Teruya Hara, Akira Date, Naoki Fujinaga, Takuji Kato, Tatsuo |
author_facet | Komatsu, Teruya Hara, Akira Date, Naoki Fujinaga, Takuji Kato, Tatsuo |
author_sort | Komatsu, Teruya |
collection | PubMed |
description | INTRODUCTION: Solitary pulmonary capillary hemangioma (SPCH) is a rare benign lung tumor that clinically resembles early lung cancer and precancerous pulmonary lesions that present with similar imaging manifestations. PRESENTATION OF CASE: The patient was a 54-year-old Japanese man who was referred to Nagara Medical Center with a ground glass opacity (GGO) lesion within the right upper lung that was incidentally detected on computed tomography. After 8 months of follow-up, video-assisted thoracoscopic segmental resection of the right upper lobe was performed with diagnostic and therapeutic intent. Pathologic examination of the resected specimen demonstrated thickening of the alveolar septum caused by the proliferation of capillary vessels. This lesion was positive for CD31 and CD34 and negative for thyroid transcription factor-1 and cytokeratin on immunohistochemical staining. The tumor was diagnosed as SPCH pathologically. DISCUSSION: When radiological examination demonstrates a GGO in the lung, SPCH must be considered as one of the differential diagnoses. For a definitive diagnosis, pathological examination of a surgically resected specimen must be conducted. CONCLUSION: This study describes a case of SPCH and a review of the literature. |
format | Online Article Text |
id | pubmed-7490444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74904442020-09-21 Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review Komatsu, Teruya Hara, Akira Date, Naoki Fujinaga, Takuji Kato, Tatsuo Int J Surg Case Rep Case Report INTRODUCTION: Solitary pulmonary capillary hemangioma (SPCH) is a rare benign lung tumor that clinically resembles early lung cancer and precancerous pulmonary lesions that present with similar imaging manifestations. PRESENTATION OF CASE: The patient was a 54-year-old Japanese man who was referred to Nagara Medical Center with a ground glass opacity (GGO) lesion within the right upper lung that was incidentally detected on computed tomography. After 8 months of follow-up, video-assisted thoracoscopic segmental resection of the right upper lobe was performed with diagnostic and therapeutic intent. Pathologic examination of the resected specimen demonstrated thickening of the alveolar septum caused by the proliferation of capillary vessels. This lesion was positive for CD31 and CD34 and negative for thyroid transcription factor-1 and cytokeratin on immunohistochemical staining. The tumor was diagnosed as SPCH pathologically. DISCUSSION: When radiological examination demonstrates a GGO in the lung, SPCH must be considered as one of the differential diagnoses. For a definitive diagnosis, pathological examination of a surgically resected specimen must be conducted. CONCLUSION: This study describes a case of SPCH and a review of the literature. Elsevier 2020-08-29 /pmc/articles/PMC7490444/ /pubmed/32916614 http://dx.doi.org/10.1016/j.ijscr.2020.08.020 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Komatsu, Teruya Hara, Akira Date, Naoki Fujinaga, Takuji Kato, Tatsuo Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review |
title | Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review |
title_full | Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review |
title_fullStr | Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review |
title_full_unstemmed | Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review |
title_short | Solitary pulmonary capillary hemangioma presenting with a ground glass opacity: A case report & literature review |
title_sort | solitary pulmonary capillary hemangioma presenting with a ground glass opacity: a case report & literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490444/ https://www.ncbi.nlm.nih.gov/pubmed/32916614 http://dx.doi.org/10.1016/j.ijscr.2020.08.020 |
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