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Posterior choroidal leiomyoma: a rare case report and literature review
We report a literature review and detailed evaluation of a rare case of posterior choroidal leiomyoma to emphasize the importance of differentiating this from other choroidal tumors. A 30‐year‐old male presented with variable blurred vision in his right eye secondary to a choroidal tumor. Clinical e...
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Published in: | APMIS : acta pathologica, microbiologica et immunologica Scandinavica microbiologica et immunologica Scandinavica, 2015-06, Vol.123 (6), p.540-545 |
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creator | Chiang, Wei‐Yu Lin, Jui‐Wei Yang, I‐Hui Kuo, Hsi‐Kung |
description | We report a literature review and detailed evaluation of a rare case of posterior choroidal leiomyoma to emphasize the importance of differentiating this from other choroidal tumors. A 30‐year‐old male presented with variable blurred vision in his right eye secondary to a choroidal tumor. Clinical examinations were performed including fundus photography, optical coherence tomography, B scans, fluorescein and indocyanine green angiography, computed tomography, and magnetic resonance imaging. Preoperative examination revealed a suspected choroidal melanoma and enucleation was performed. However, a definitive diagnosis of choroidal leiomyoma was made following postoperative pathological light microscopy and immunohistochemical studies. Published case reports were collected and the common characteristics and distinctive features were compared with the current case. Posterior choroidal leiomyoma was summarized from the literature, and beneficial information for diagnosis and treatment was obtained. In conclusion, posterior choroidal leiomyoma is rare and should be differentiated from amelanotic melanomas. Despite the benign nature, an explanation regarding the rare incidence and difficult diagnosis of posterior choroidal leiomyoma must be provided to patients, prior to enucleation or detrimental treatment. |
doi_str_mv | 10.1111/apm.12384 |
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A 30‐year‐old male presented with variable blurred vision in his right eye secondary to a choroidal tumor. Clinical examinations were performed including fundus photography, optical coherence tomography, B scans, fluorescein and indocyanine green angiography, computed tomography, and magnetic resonance imaging. Preoperative examination revealed a suspected choroidal melanoma and enucleation was performed. However, a definitive diagnosis of choroidal leiomyoma was made following postoperative pathological light microscopy and immunohistochemical studies. Published case reports were collected and the common characteristics and distinctive features were compared with the current case. Posterior choroidal leiomyoma was summarized from the literature, and beneficial information for diagnosis and treatment was obtained. In conclusion, posterior choroidal leiomyoma is rare and should be differentiated from amelanotic melanomas. Despite the benign nature, an explanation regarding the rare incidence and difficult diagnosis of posterior choroidal leiomyoma must be provided to patients, prior to enucleation or detrimental treatment.</description><identifier>ISSN: 0903-4641</identifier><identifier>EISSN: 1600-0463</identifier><identifier>DOI: 10.1111/apm.12384</identifier><identifier>PMID: 25907891</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Adult ; Choroid Neoplasms - diagnosis ; Choroid Neoplasms - pathology ; Choroid Neoplasms - therapy ; Choroidal leiomyoma ; choroidal tumor ; Fibroids ; Humans ; Leiomyoma - diagnosis ; Leiomyoma - pathology ; Leiomyoma - therapy ; Literature reviews ; Male ; Melanoma - diagnosis ; Melanoma - pathology ; Melanoma - therapy ; Skin cancer ; smooth muscle tumor ; Tomography ; Uveal Neoplasms - diagnosis ; Uveal Neoplasms - pathology ; Uveal Neoplasms - therapy</subject><ispartof>APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2015-06, Vol.123 (6), p.540-545</ispartof><rights>2015 APMIS. 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A 30‐year‐old male presented with variable blurred vision in his right eye secondary to a choroidal tumor. Clinical examinations were performed including fundus photography, optical coherence tomography, B scans, fluorescein and indocyanine green angiography, computed tomography, and magnetic resonance imaging. Preoperative examination revealed a suspected choroidal melanoma and enucleation was performed. However, a definitive diagnosis of choroidal leiomyoma was made following postoperative pathological light microscopy and immunohistochemical studies. Published case reports were collected and the common characteristics and distinctive features were compared with the current case. Posterior choroidal leiomyoma was summarized from the literature, and beneficial information for diagnosis and treatment was obtained. In conclusion, posterior choroidal leiomyoma is rare and should be differentiated from amelanotic melanomas. Despite the benign nature, an explanation regarding the rare incidence and difficult diagnosis of posterior choroidal leiomyoma must be provided to patients, prior to enucleation or detrimental treatment.</description><subject>Adult</subject><subject>Choroid Neoplasms - diagnosis</subject><subject>Choroid Neoplasms - pathology</subject><subject>Choroid Neoplasms - therapy</subject><subject>Choroidal leiomyoma</subject><subject>choroidal tumor</subject><subject>Fibroids</subject><subject>Humans</subject><subject>Leiomyoma - diagnosis</subject><subject>Leiomyoma - pathology</subject><subject>Leiomyoma - therapy</subject><subject>Literature reviews</subject><subject>Male</subject><subject>Melanoma - diagnosis</subject><subject>Melanoma - pathology</subject><subject>Melanoma - therapy</subject><subject>Skin cancer</subject><subject>smooth muscle tumor</subject><subject>Tomography</subject><subject>Uveal Neoplasms - diagnosis</subject><subject>Uveal Neoplasms - pathology</subject><subject>Uveal Neoplasms - therapy</subject><issn>0903-4641</issn><issn>1600-0463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp10E9LwzAYBvAgipvTg19AAl700C1p_rXextApTNxBzyVt3mJGu8ykdezb29npQTCXF8LvfXh5ELqkZEy7N9GbekxjlvAjNKSSkIhwyY7RkKSERVxyOkBnIawIoXEi1SkaxCIlKknpEM2XLjTgrfO4eHfeWaMrXIF19c7V-g5r7LUHXOgA2MPG-QbrtcGV7ZZ00_r976eF7Tk6KXUV4OIwR-jt4f519hgtXuZPs-kiKnjMeMRMkXAlTUmBMiqEFAkDooUpTZ6rRBqQHMDEpFTAtU610JKzVOYglTBEshG66XM33n20EJqstqGAqtJrcG3IqEyYEixlcUev_9CVa_26u26vYqFiqUinbntVeBeChzLbeFtrv8soyfbtZl272Xe7nb06JLZ5DeZX_tTZgUkPtraC3f9J2XT53Ed-Aa3oguU</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Chiang, Wei‐Yu</creator><creator>Lin, Jui‐Wei</creator><creator>Yang, I‐Hui</creator><creator>Kuo, Hsi‐Kung</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>7T7</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201506</creationdate><title>Posterior choroidal leiomyoma: a rare case report and literature review</title><author>Chiang, Wei‐Yu ; 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A 30‐year‐old male presented with variable blurred vision in his right eye secondary to a choroidal tumor. Clinical examinations were performed including fundus photography, optical coherence tomography, B scans, fluorescein and indocyanine green angiography, computed tomography, and magnetic resonance imaging. Preoperative examination revealed a suspected choroidal melanoma and enucleation was performed. However, a definitive diagnosis of choroidal leiomyoma was made following postoperative pathological light microscopy and immunohistochemical studies. Published case reports were collected and the common characteristics and distinctive features were compared with the current case. Posterior choroidal leiomyoma was summarized from the literature, and beneficial information for diagnosis and treatment was obtained. In conclusion, posterior choroidal leiomyoma is rare and should be differentiated from amelanotic melanomas. Despite the benign nature, an explanation regarding the rare incidence and difficult diagnosis of posterior choroidal leiomyoma must be provided to patients, prior to enucleation or detrimental treatment.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>25907891</pmid><doi>10.1111/apm.12384</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Choroid Neoplasms - diagnosis Choroid Neoplasms - pathology Choroid Neoplasms - therapy Choroidal leiomyoma choroidal tumor Fibroids Humans Leiomyoma - diagnosis Leiomyoma - pathology Leiomyoma - therapy Literature reviews Male Melanoma - diagnosis Melanoma - pathology Melanoma - therapy Skin cancer smooth muscle tumor Tomography Uveal Neoplasms - diagnosis Uveal Neoplasms - pathology Uveal Neoplasms - therapy |
title | Posterior choroidal leiomyoma: a rare case report and literature review |
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