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An unusual case report of multiple pulmonary leiomyomatous hamartoma
RATIONALE: Multiple pulmonary leiomyomatous hamartoma (MPLH) is an extremely rare benign disease that mostly occurs in women of reproductive age. PATIENT CONCERNS: A 32-year-old female patient recently diagnosed with multiple bilateral pulmonary nodules. She has the symptoms of dry cough, chest tigh...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709040/ https://www.ncbi.nlm.nih.gov/pubmed/31348260 http://dx.doi.org/10.1097/MD.0000000000016496 |
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author | Cheng, Dan Zhang, Fangcheng Hu, Ke |
author_facet | Cheng, Dan Zhang, Fangcheng Hu, Ke |
author_sort | Cheng, Dan |
collection | PubMed |
description | RATIONALE: Multiple pulmonary leiomyomatous hamartoma (MPLH) is an extremely rare benign disease that mostly occurs in women of reproductive age. PATIENT CONCERNS: A 32-year-old female patient recently diagnosed with multiple bilateral pulmonary nodules. She has the symptoms of dry cough, chest tightness, dyspnea on exertion. Chest X-ray identified multiple bilateral pulmonary nodules in the lung, and the diameter of the largest nodule was about 3.1 cm. DIAGNOSES: Pathology confirmed the diagnosis of MPLH based on morphology and immunohistochemical staining. INTERVENTIONS: The patient presented with multiple well-defined nodular shadows in chest computed tomography (CT), atypical image and symptoms were detected. Positron emission tomography/CT scan showed mild fluorine-18 fluorodeoxyglucose uptake in the lesions and no abnormal foci in any other parts of her body. She subsequently underwent a video-assisted thoracoscopic surgery with wedge resection of the biggest one of the nodules. Then the patient given symptomatic treatment, without hormone, no further treatment was prescribed. OUTCOMES: The patient is in the good general condition and without obvious pulmonary symptoms after the follow-up of 1 year, chest CT scan showed no significant changes in the sizes and locations of her bilateral pulmonary nodules. LESSONS: Due to its rare presentation, the primary MPLH may be undiagnosed. Awareness of main morphologic and immunohistochemical features of MPLH is critical for the recognition of this uncommon disease. |
format | Online Article Text |
id | pubmed-6709040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-67090402019-10-01 An unusual case report of multiple pulmonary leiomyomatous hamartoma Cheng, Dan Zhang, Fangcheng Hu, Ke Medicine (Baltimore) Research Article RATIONALE: Multiple pulmonary leiomyomatous hamartoma (MPLH) is an extremely rare benign disease that mostly occurs in women of reproductive age. PATIENT CONCERNS: A 32-year-old female patient recently diagnosed with multiple bilateral pulmonary nodules. She has the symptoms of dry cough, chest tightness, dyspnea on exertion. Chest X-ray identified multiple bilateral pulmonary nodules in the lung, and the diameter of the largest nodule was about 3.1 cm. DIAGNOSES: Pathology confirmed the diagnosis of MPLH based on morphology and immunohistochemical staining. INTERVENTIONS: The patient presented with multiple well-defined nodular shadows in chest computed tomography (CT), atypical image and symptoms were detected. Positron emission tomography/CT scan showed mild fluorine-18 fluorodeoxyglucose uptake in the lesions and no abnormal foci in any other parts of her body. She subsequently underwent a video-assisted thoracoscopic surgery with wedge resection of the biggest one of the nodules. Then the patient given symptomatic treatment, without hormone, no further treatment was prescribed. OUTCOMES: The patient is in the good general condition and without obvious pulmonary symptoms after the follow-up of 1 year, chest CT scan showed no significant changes in the sizes and locations of her bilateral pulmonary nodules. LESSONS: Due to its rare presentation, the primary MPLH may be undiagnosed. Awareness of main morphologic and immunohistochemical features of MPLH is critical for the recognition of this uncommon disease. Wolters Kluwer Health 2019-07-26 /pmc/articles/PMC6709040/ /pubmed/31348260 http://dx.doi.org/10.1097/MD.0000000000016496 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Research Article Cheng, Dan Zhang, Fangcheng Hu, Ke An unusual case report of multiple pulmonary leiomyomatous hamartoma |
title | An unusual case report of multiple pulmonary leiomyomatous hamartoma |
title_full | An unusual case report of multiple pulmonary leiomyomatous hamartoma |
title_fullStr | An unusual case report of multiple pulmonary leiomyomatous hamartoma |
title_full_unstemmed | An unusual case report of multiple pulmonary leiomyomatous hamartoma |
title_short | An unusual case report of multiple pulmonary leiomyomatous hamartoma |
title_sort | unusual case report of multiple pulmonary leiomyomatous hamartoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709040/ https://www.ncbi.nlm.nih.gov/pubmed/31348260 http://dx.doi.org/10.1097/MD.0000000000016496 |
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