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A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage

Conjunctival amyloidosis is a very rare disease, and its presence may be a sign of systemic amyloidosis. We present our ocular and systemic findings in a patient with conjunctival amyloidosis. A 43-year-old man had repeated subconjunctival hemorrhages (SCHs) for two years and was referred to the Chi...

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Autores principales: Ando, Takaaki, Oshitari, Toshiyuki, Saito, Mamiko, Tawada, Ayako, Baba, Takayuki, Yotsukura, Jiro, Yamamoto, Shuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343237/
https://www.ncbi.nlm.nih.gov/pubmed/28326212
http://dx.doi.org/10.1155/2017/5423027
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author Ando, Takaaki
Oshitari, Toshiyuki
Saito, Mamiko
Tawada, Ayako
Baba, Takayuki
Yotsukura, Jiro
Yamamoto, Shuichi
author_facet Ando, Takaaki
Oshitari, Toshiyuki
Saito, Mamiko
Tawada, Ayako
Baba, Takayuki
Yotsukura, Jiro
Yamamoto, Shuichi
author_sort Ando, Takaaki
collection PubMed
description Conjunctival amyloidosis is a very rare disease, and its presence may be a sign of systemic amyloidosis. We present our ocular and systemic findings in a patient with conjunctival amyloidosis. A 43-year-old man had repeated subconjunctival hemorrhages (SCHs) for two years and was referred to the Chiba University Hospital. He had comprehensive ophthalmological and systemic examinations to determine the cause of the SCHs. His visual acuities were 1.2 OU, and the intraocular pressures were 13-14 mmHg OU. Magnetic resonance imaging was normal. Initially, the SCH was the only abnormality. After 3 months, the SCH had partially cleared, and a pink mass was detected in the superior area of the subconjunctiva. Partial biopsy and histopathological examinations showed a greenish birefringence and dichroism under polarized light illumination. The birefringence was located in amyloid fibers. Immunofixation electrophoresis detected λ-light chain abnormality in the ocular biopsy specimen but systemic examinations did not find any lesions. Multiple myeloma was ruled out, and the patient is being followed closely to detect any early signs of systemic amyloidosis. Because repeated SCHs might be initial signs of systemic amyloidosis, patients with conjunctival amyloidosis should be comprehensively examined for systemic amyloidosis because of its poor life prognosis.
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spelling pubmed-53432372017-03-21 A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage Ando, Takaaki Oshitari, Toshiyuki Saito, Mamiko Tawada, Ayako Baba, Takayuki Yotsukura, Jiro Yamamoto, Shuichi Case Rep Ophthalmol Med Case Report Conjunctival amyloidosis is a very rare disease, and its presence may be a sign of systemic amyloidosis. We present our ocular and systemic findings in a patient with conjunctival amyloidosis. A 43-year-old man had repeated subconjunctival hemorrhages (SCHs) for two years and was referred to the Chiba University Hospital. He had comprehensive ophthalmological and systemic examinations to determine the cause of the SCHs. His visual acuities were 1.2 OU, and the intraocular pressures were 13-14 mmHg OU. Magnetic resonance imaging was normal. Initially, the SCH was the only abnormality. After 3 months, the SCH had partially cleared, and a pink mass was detected in the superior area of the subconjunctiva. Partial biopsy and histopathological examinations showed a greenish birefringence and dichroism under polarized light illumination. The birefringence was located in amyloid fibers. Immunofixation electrophoresis detected λ-light chain abnormality in the ocular biopsy specimen but systemic examinations did not find any lesions. Multiple myeloma was ruled out, and the patient is being followed closely to detect any early signs of systemic amyloidosis. Because repeated SCHs might be initial signs of systemic amyloidosis, patients with conjunctival amyloidosis should be comprehensively examined for systemic amyloidosis because of its poor life prognosis. Hindawi Publishing Corporation 2017 2017-02-23 /pmc/articles/PMC5343237/ /pubmed/28326212 http://dx.doi.org/10.1155/2017/5423027 Text en Copyright © 2017 Takaaki Ando et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ando, Takaaki
Oshitari, Toshiyuki
Saito, Mamiko
Tawada, Ayako
Baba, Takayuki
Yotsukura, Jiro
Yamamoto, Shuichi
A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage
title A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage
title_full A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage
title_fullStr A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage
title_full_unstemmed A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage
title_short A Case of Conjunctival Amyloidosis with Repeated Subconjunctival Hemorrhage
title_sort case of conjunctival amyloidosis with repeated subconjunctival hemorrhage
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343237/
https://www.ncbi.nlm.nih.gov/pubmed/28326212
http://dx.doi.org/10.1155/2017/5423027
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