A case of protein-losing gastroenteropathy due to Sjögren’s syndrome detected by foggy vision with refractive error of the intraocular lens
A woman in her forties visited an ophthalmologist for rapidly progressive foggy vision. Naked visual acuity had decreased to 0.15, and although her eyes showed no abnormalities, internal disease was suspected and albumin 2.6 g/dL was found. Protein leakage from the intestinal tract was suspected sin...
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Veröffentlicht in: | Clinical journal of gastroenterology 2024-12, Vol.17 (6), p.1039-1046 |
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creator | Watanabe, Naho Kaneko, Rena Kishi, Monami Yanai, Ryo Ikehara, Takashi Nagai, Hidenari Matsuda, Takahisa |
description | A woman in her forties visited an ophthalmologist for rapidly progressive foggy vision. Naked visual acuity had decreased to 0.15, and although her eyes showed no abnormalities, internal disease was suspected and albumin 2.6 g/dL was found. Protein leakage from the intestinal tract was suspected since there was no urinary protein excretion.
99m
Technetium-labeled albumin D scintigraphy showed protein leakage from the intestinal tract. A stool α1-antitrypsin clearance test showed an increase to 56.3 mL/day, leading to a diagnosis of protein-losing gastroenteropathy. Blood biochemistry revealed abnormally high levels of anti-SS-A and anti-SS-B antibodies (≥ 1200 U/mL and ≥ 1000 U/mL, respectively). A lip salivary gland biopsy revealed lymphocytic infiltrate at least 1 focus per 2 mm × 2 mm > 50 lymphocytes per conduit). The Schirmer test result was 5 mm/5 min or less, which led to the diagnosis of Sjögren’s syndrome. The serum albumin level increased with intravenous administration of methylprednisolone 50 mg (1 mg/kg), and the patient is currently on oral prednisolone at a gradually decreasing dose. After administration of prednisolone, visual acuity recovered to 1.2 with recovery of albumin. |
doi_str_mv | 10.1007/s12328-024-02038-2 |
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99m
Technetium-labeled albumin D scintigraphy showed protein leakage from the intestinal tract. A stool α1-antitrypsin clearance test showed an increase to 56.3 mL/day, leading to a diagnosis of protein-losing gastroenteropathy. Blood biochemistry revealed abnormally high levels of anti-SS-A and anti-SS-B antibodies (≥ 1200 U/mL and ≥ 1000 U/mL, respectively). A lip salivary gland biopsy revealed lymphocytic infiltrate at least 1 focus per 2 mm × 2 mm > 50 lymphocytes per conduit). The Schirmer test result was 5 mm/5 min or less, which led to the diagnosis of Sjögren’s syndrome. The serum albumin level increased with intravenous administration of methylprednisolone 50 mg (1 mg/kg), and the patient is currently on oral prednisolone at a gradually decreasing dose. After administration of prednisolone, visual acuity recovered to 1.2 with recovery of albumin.</description><identifier>ISSN: 1865-7257</identifier><identifier>ISSN: 1865-7265</identifier><identifier>EISSN: 1865-7265</identifier><identifier>DOI: 10.1007/s12328-024-02038-2</identifier><identifier>PMID: 39297920</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Abdominal Surgery ; Antibodies, Antinuclear - blood ; Case Report ; Colorectal Surgery ; Female ; Gastroenterology ; Hepatology ; Humans ; Medicine ; Medicine & Public Health ; Middle Aged ; Protein-Losing Enteropathies - diagnosis ; Protein-Losing Enteropathies - etiology ; Sjogren's Syndrome - complications ; Sjogren's Syndrome - diagnosis ; Surgical Oncology ; Vision Disorders - etiology</subject><ispartof>Clinical journal of gastroenterology, 2024-12, Vol.17 (6), p.1039-1046</ispartof><rights>Japanese Society of Gastroenterology 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. Japanese Society of Gastroenterology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c228t-843cc5fb569f0de339bb173d6540eb95ca25520428511f4a7c8b417d977980853</cites><orcidid>0000-0002-0044-1821</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12328-024-02038-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12328-024-02038-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39297920$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Watanabe, Naho</creatorcontrib><creatorcontrib>Kaneko, Rena</creatorcontrib><creatorcontrib>Kishi, Monami</creatorcontrib><creatorcontrib>Yanai, Ryo</creatorcontrib><creatorcontrib>Ikehara, Takashi</creatorcontrib><creatorcontrib>Nagai, Hidenari</creatorcontrib><creatorcontrib>Matsuda, Takahisa</creatorcontrib><title>A case of protein-losing gastroenteropathy due to Sjögren’s syndrome detected by foggy vision with refractive error of the intraocular lens</title><title>Clinical journal of gastroenterology</title><addtitle>Clin J Gastroenterol</addtitle><addtitle>Clin J Gastroenterol</addtitle><description>A woman in her forties visited an ophthalmologist for rapidly progressive foggy vision. Naked visual acuity had decreased to 0.15, and although her eyes showed no abnormalities, internal disease was suspected and albumin 2.6 g/dL was found. Protein leakage from the intestinal tract was suspected since there was no urinary protein excretion.
99m
Technetium-labeled albumin D scintigraphy showed protein leakage from the intestinal tract. A stool α1-antitrypsin clearance test showed an increase to 56.3 mL/day, leading to a diagnosis of protein-losing gastroenteropathy. Blood biochemistry revealed abnormally high levels of anti-SS-A and anti-SS-B antibodies (≥ 1200 U/mL and ≥ 1000 U/mL, respectively). A lip salivary gland biopsy revealed lymphocytic infiltrate at least 1 focus per 2 mm × 2 mm > 50 lymphocytes per conduit). The Schirmer test result was 5 mm/5 min or less, which led to the diagnosis of Sjögren’s syndrome. The serum albumin level increased with intravenous administration of methylprednisolone 50 mg (1 mg/kg), and the patient is currently on oral prednisolone at a gradually decreasing dose. After administration of prednisolone, visual acuity recovered to 1.2 with recovery of albumin.</description><subject>Abdominal Surgery</subject><subject>Antibodies, Antinuclear - blood</subject><subject>Case Report</subject><subject>Colorectal Surgery</subject><subject>Female</subject><subject>Gastroenterology</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Protein-Losing Enteropathies - diagnosis</subject><subject>Protein-Losing Enteropathies - etiology</subject><subject>Sjogren's Syndrome - complications</subject><subject>Sjogren's Syndrome - diagnosis</subject><subject>Surgical Oncology</subject><subject>Vision Disorders - etiology</subject><issn>1865-7257</issn><issn>1865-7265</issn><issn>1865-7265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UUtuFTEQtBARCYELsEBeshnwZzy2l1EECVIkFoS15fH0zPPTPPthe4JmlxOwz0VyAW7CSXB4IUsWrW6pq6pVXQi9oeQ9JUR-yJRxphrC2lqEq4Y9QydUdaKRrBPPn2Yhj9HLnLeEdIxI_gIdc8201IycoJ9n2NkMOI54n2IBH5o5Zh8mPNlcUoRQIMW9LZsVDwvgEvHX7a_7KUH4fXuXcV7DkOIO8AAFXIEB9yse4zSt-MZnHwP-4csGJxiTdcXfAIaUYnq4VzaAfSjJRrfMNuEZQn6FjkY7Z3j92E_Rt08fr88vm6svF5_Pz64ax5gqjWq5c2LsRadHMgDnuu-p5EMnWgK9Fs4yIRhpmRKUjq2VTvUtlYOWUiuiBD9F7w661fT3BXIxO58dzLMNEJdsOCWSilYxXaHsAHUp5lyNmH3yO5tWQ4l5yMEccjA1B_M3B8Mq6e2j_tLvYHii_Ht8BfADINdVmCCZbVxSqJ7_J_sHSnmXIQ</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Watanabe, Naho</creator><creator>Kaneko, Rena</creator><creator>Kishi, Monami</creator><creator>Yanai, Ryo</creator><creator>Ikehara, Takashi</creator><creator>Nagai, Hidenari</creator><creator>Matsuda, Takahisa</creator><general>Springer Nature Singapore</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>7X8</scope><orcidid>https://orcid.org/0000-0002-0044-1821</orcidid></search><sort><creationdate>20241201</creationdate><title>A case of protein-losing gastroenteropathy due to Sjögren’s syndrome detected by foggy vision with refractive error of the intraocular lens</title><author>Watanabe, Naho ; Kaneko, Rena ; Kishi, Monami ; Yanai, Ryo ; Ikehara, Takashi ; Nagai, Hidenari ; Matsuda, Takahisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c228t-843cc5fb569f0de339bb173d6540eb95ca25520428511f4a7c8b417d977980853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Abdominal Surgery</topic><topic>Antibodies, Antinuclear - blood</topic><topic>Case Report</topic><topic>Colorectal Surgery</topic><topic>Female</topic><topic>Gastroenterology</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Protein-Losing Enteropathies - diagnosis</topic><topic>Protein-Losing Enteropathies - etiology</topic><topic>Sjogren's Syndrome - complications</topic><topic>Sjogren's Syndrome - diagnosis</topic><topic>Surgical Oncology</topic><topic>Vision Disorders - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Watanabe, Naho</creatorcontrib><creatorcontrib>Kaneko, Rena</creatorcontrib><creatorcontrib>Kishi, Monami</creatorcontrib><creatorcontrib>Yanai, Ryo</creatorcontrib><creatorcontrib>Ikehara, Takashi</creatorcontrib><creatorcontrib>Nagai, Hidenari</creatorcontrib><creatorcontrib>Matsuda, Takahisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watanabe, Naho</au><au>Kaneko, Rena</au><au>Kishi, Monami</au><au>Yanai, Ryo</au><au>Ikehara, Takashi</au><au>Nagai, Hidenari</au><au>Matsuda, Takahisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of protein-losing gastroenteropathy due to Sjögren’s syndrome detected by foggy vision with refractive error of the intraocular lens</atitle><jtitle>Clinical journal of gastroenterology</jtitle><stitle>Clin J Gastroenterol</stitle><addtitle>Clin J Gastroenterol</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>17</volume><issue>6</issue><spage>1039</spage><epage>1046</epage><pages>1039-1046</pages><issn>1865-7257</issn><issn>1865-7265</issn><eissn>1865-7265</eissn><abstract>A woman in her forties visited an ophthalmologist for rapidly progressive foggy vision. Naked visual acuity had decreased to 0.15, and although her eyes showed no abnormalities, internal disease was suspected and albumin 2.6 g/dL was found. Protein leakage from the intestinal tract was suspected since there was no urinary protein excretion.
99m
Technetium-labeled albumin D scintigraphy showed protein leakage from the intestinal tract. A stool α1-antitrypsin clearance test showed an increase to 56.3 mL/day, leading to a diagnosis of protein-losing gastroenteropathy. Blood biochemistry revealed abnormally high levels of anti-SS-A and anti-SS-B antibodies (≥ 1200 U/mL and ≥ 1000 U/mL, respectively). A lip salivary gland biopsy revealed lymphocytic infiltrate at least 1 focus per 2 mm × 2 mm > 50 lymphocytes per conduit). The Schirmer test result was 5 mm/5 min or less, which led to the diagnosis of Sjögren’s syndrome. The serum albumin level increased with intravenous administration of methylprednisolone 50 mg (1 mg/kg), and the patient is currently on oral prednisolone at a gradually decreasing dose. After administration of prednisolone, visual acuity recovered to 1.2 with recovery of albumin.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>39297920</pmid><doi>10.1007/s12328-024-02038-2</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0044-1821</orcidid></addata></record> |
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subjects | Abdominal Surgery Antibodies, Antinuclear - blood Case Report Colorectal Surgery Female Gastroenterology Hepatology Humans Medicine Medicine & Public Health Middle Aged Protein-Losing Enteropathies - diagnosis Protein-Losing Enteropathies - etiology Sjogren's Syndrome - complications Sjogren's Syndrome - diagnosis Surgical Oncology Vision Disorders - etiology |
title | A case of protein-losing gastroenteropathy due to Sjögren’s syndrome detected by foggy vision with refractive error of the intraocular lens |
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