Intestinal Lymphangiectasia: Insights on Management and Literature Review

BACKGROUND Intestinal lymphangiectasia (IL) is a rare disease characterized by a dilatation of the intestinal lymphatics and loss of lymph fluid into the gastrointestinal tract leading to hypoproteinemia, edema, lymphocytopenia, hypogammaglobinemia, and immunological abnormalities. Iron, calcium, an...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The American journal of case reports 2016-07, Vol.17, p.512-522
Hauptverfasser: Alshikho, Mohamad J, Talas, Joud M, Noureldine, Salem I, Zazou, Saf, Addas, Aladdin, Kurabi, Haitham, Nasser, Mahmoud
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 522
container_issue
container_start_page 512
container_title The American journal of case reports
container_volume 17
creator Alshikho, Mohamad J
Talas, Joud M
Noureldine, Salem I
Zazou, Saf
Addas, Aladdin
Kurabi, Haitham
Nasser, Mahmoud
description BACKGROUND Intestinal lymphangiectasia (IL) is a rare disease characterized by a dilatation of the intestinal lymphatics and loss of lymph fluid into the gastrointestinal tract leading to hypoproteinemia, edema, lymphocytopenia, hypogammaglobinemia, and immunological abnormalities. Iron, calcium, and other serum components (e.g., lipids, fat soluble vitamins) may also be depleted. A literature search revealed more than 200 reported cases of IL. Herein, we report our observations of a patient diagnosed with IL; we also present our conclusion for our review of the published literature. CASE REPORT A 24-year-old male was admitted to Aleppo University Hospital with the complaints of abdominal pain, headache, arthralgia, fever, and rigors. His past medical history was remarkable for frequent episodes of diarrhea, recurrent infections, and swelling in the lower limbs. In addition, he had been hospitalized several times in non-academic hospitals due to edema in his legs, cellulitis, and recurrent infections. In the emergency department, a physical examination revealed a patient in distress. He was weak, dehydrated, pale, and had a high-grade fever. His lower extremities were edematous, swollen, and extremely tender to touch. The overlying skin was erythematous and warm. Moreover, the patient was tachycardic, tacypneic, and moderately hypotensive. The patient was resuscitated with IV fluids, and Tylenol was administered to bring the temperature down. Blood tests showed anemia and high levels of inflammatory markers. The patient's white blood cell count was elevated with an obvious left shift. However, subsequent investigations showed that the patient had IL. Suitable diet modification plans were applied as a long-term management plan. CONCLUSIONS IL is a rare disease of challenging nature due to its systematic effects and lack of comprehensive studies that can evaluate the effectiveness of specific treatments in a large cohort of patients. MCT (medium-chain triglyceride) oils and diet modification strategies are effective in reducing the loss of body proteins and in maintaining near-normal blood levels of immunoglobulins. However, octreotide and MCT oils had no proven role in shrinking edema in our patient.
doi_str_mv 10.12659/AJCR.899636
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4957630</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1806445573</sourcerecordid><originalsourceid>FETCH-LOGICAL-c384t-cb2bb79e242fc2cc9f6ec8c55fa3d7b2e33d22c24c9b2058ee5b3a868f15209f3</originalsourceid><addsrcrecordid>eNpVkctLw0AQxhdRbKm9eZYcPZia7CtZD4IUH5GIUPS8bDaTdCXZ1GxS6X9vtLXUuczA_Pjm8SF0HgazEHMmru-e54tZLAQn_AiNQ0FDnwlMjg_qEZo69xEMwTGPMDlFIxxRGuAoGqMksR24zlhVeemmXi2VLQ3oTjmjbrzEOlMuO-c11ntRVpVQg-08ZXMvNR20qutb8BawNvB1hk4KVTmY7vIEvT_cv82f_PT1MZnfpb4mMe18neEsiwRgiguNtRYFBx1rxgpF8ijDQEiOscZUiwwHLAZgGVExj4uQ4UAUZIJut7qrPqsh18NCrarkqjW1ajeyUUb-71izlGWzllSwiJNgELjcCbTNZz8cL2vjNFSVstD0ToZxwCllLCIDerVFdds410KxHxMG8tcA-WOA3Bow4BeHq-3hv3eTbxAXgpc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1806445573</pqid></control><display><type>article</type><title>Intestinal Lymphangiectasia: Insights on Management and Literature Review</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Alshikho, Mohamad J ; Talas, Joud M ; Noureldine, Salem I ; Zazou, Saf ; Addas, Aladdin ; Kurabi, Haitham ; Nasser, Mahmoud</creator><creatorcontrib>Alshikho, Mohamad J ; Talas, Joud M ; Noureldine, Salem I ; Zazou, Saf ; Addas, Aladdin ; Kurabi, Haitham ; Nasser, Mahmoud</creatorcontrib><description>BACKGROUND Intestinal lymphangiectasia (IL) is a rare disease characterized by a dilatation of the intestinal lymphatics and loss of lymph fluid into the gastrointestinal tract leading to hypoproteinemia, edema, lymphocytopenia, hypogammaglobinemia, and immunological abnormalities. Iron, calcium, and other serum components (e.g., lipids, fat soluble vitamins) may also be depleted. A literature search revealed more than 200 reported cases of IL. Herein, we report our observations of a patient diagnosed with IL; we also present our conclusion for our review of the published literature. CASE REPORT A 24-year-old male was admitted to Aleppo University Hospital with the complaints of abdominal pain, headache, arthralgia, fever, and rigors. His past medical history was remarkable for frequent episodes of diarrhea, recurrent infections, and swelling in the lower limbs. In addition, he had been hospitalized several times in non-academic hospitals due to edema in his legs, cellulitis, and recurrent infections. In the emergency department, a physical examination revealed a patient in distress. He was weak, dehydrated, pale, and had a high-grade fever. His lower extremities were edematous, swollen, and extremely tender to touch. The overlying skin was erythematous and warm. Moreover, the patient was tachycardic, tacypneic, and moderately hypotensive. The patient was resuscitated with IV fluids, and Tylenol was administered to bring the temperature down. Blood tests showed anemia and high levels of inflammatory markers. The patient's white blood cell count was elevated with an obvious left shift. However, subsequent investigations showed that the patient had IL. Suitable diet modification plans were applied as a long-term management plan. CONCLUSIONS IL is a rare disease of challenging nature due to its systematic effects and lack of comprehensive studies that can evaluate the effectiveness of specific treatments in a large cohort of patients. MCT (medium-chain triglyceride) oils and diet modification strategies are effective in reducing the loss of body proteins and in maintaining near-normal blood levels of immunoglobulins. However, octreotide and MCT oils had no proven role in shrinking edema in our patient.</description><identifier>ISSN: 1941-5923</identifier><identifier>EISSN: 1941-5923</identifier><identifier>DOI: 10.12659/AJCR.899636</identifier><identifier>PMID: 27440277</identifier><language>eng</language><publisher>United States: International Scientific Literature, Inc</publisher><subject>Biopsy ; Diagnosis, Differential ; Diarrhea - diagnosis ; Diarrhea - etiology ; Diarrhea - therapy ; Disease Management ; Endoscopy, Digestive System ; Humans ; Intestines - diagnostic imaging ; Lymphangiectasis, Intestinal - complications ; Lymphangiectasis, Intestinal - diagnosis ; Lymphangiectasis, Intestinal - therapy ; Male ; Radiography, Abdominal ; Tomography, X-Ray Computed ; Ultrasonography ; Young Adult</subject><ispartof>The American journal of case reports, 2016-07, Vol.17, p.512-522</ispartof><rights>Am J Case Rep, 2016 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-cb2bb79e242fc2cc9f6ec8c55fa3d7b2e33d22c24c9b2058ee5b3a868f15209f3</citedby><cites>FETCH-LOGICAL-c384t-cb2bb79e242fc2cc9f6ec8c55fa3d7b2e33d22c24c9b2058ee5b3a868f15209f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957630/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957630/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27440277$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alshikho, Mohamad J</creatorcontrib><creatorcontrib>Talas, Joud M</creatorcontrib><creatorcontrib>Noureldine, Salem I</creatorcontrib><creatorcontrib>Zazou, Saf</creatorcontrib><creatorcontrib>Addas, Aladdin</creatorcontrib><creatorcontrib>Kurabi, Haitham</creatorcontrib><creatorcontrib>Nasser, Mahmoud</creatorcontrib><title>Intestinal Lymphangiectasia: Insights on Management and Literature Review</title><title>The American journal of case reports</title><addtitle>Am J Case Rep</addtitle><description>BACKGROUND Intestinal lymphangiectasia (IL) is a rare disease characterized by a dilatation of the intestinal lymphatics and loss of lymph fluid into the gastrointestinal tract leading to hypoproteinemia, edema, lymphocytopenia, hypogammaglobinemia, and immunological abnormalities. Iron, calcium, and other serum components (e.g., lipids, fat soluble vitamins) may also be depleted. A literature search revealed more than 200 reported cases of IL. Herein, we report our observations of a patient diagnosed with IL; we also present our conclusion for our review of the published literature. CASE REPORT A 24-year-old male was admitted to Aleppo University Hospital with the complaints of abdominal pain, headache, arthralgia, fever, and rigors. His past medical history was remarkable for frequent episodes of diarrhea, recurrent infections, and swelling in the lower limbs. In addition, he had been hospitalized several times in non-academic hospitals due to edema in his legs, cellulitis, and recurrent infections. In the emergency department, a physical examination revealed a patient in distress. He was weak, dehydrated, pale, and had a high-grade fever. His lower extremities were edematous, swollen, and extremely tender to touch. The overlying skin was erythematous and warm. Moreover, the patient was tachycardic, tacypneic, and moderately hypotensive. The patient was resuscitated with IV fluids, and Tylenol was administered to bring the temperature down. Blood tests showed anemia and high levels of inflammatory markers. The patient's white blood cell count was elevated with an obvious left shift. However, subsequent investigations showed that the patient had IL. Suitable diet modification plans were applied as a long-term management plan. CONCLUSIONS IL is a rare disease of challenging nature due to its systematic effects and lack of comprehensive studies that can evaluate the effectiveness of specific treatments in a large cohort of patients. MCT (medium-chain triglyceride) oils and diet modification strategies are effective in reducing the loss of body proteins and in maintaining near-normal blood levels of immunoglobulins. However, octreotide and MCT oils had no proven role in shrinking edema in our patient.</description><subject>Biopsy</subject><subject>Diagnosis, Differential</subject><subject>Diarrhea - diagnosis</subject><subject>Diarrhea - etiology</subject><subject>Diarrhea - therapy</subject><subject>Disease Management</subject><subject>Endoscopy, Digestive System</subject><subject>Humans</subject><subject>Intestines - diagnostic imaging</subject><subject>Lymphangiectasis, Intestinal - complications</subject><subject>Lymphangiectasis, Intestinal - diagnosis</subject><subject>Lymphangiectasis, Intestinal - therapy</subject><subject>Male</subject><subject>Radiography, Abdominal</subject><subject>Tomography, X-Ray Computed</subject><subject>Ultrasonography</subject><subject>Young Adult</subject><issn>1941-5923</issn><issn>1941-5923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctLw0AQxhdRbKm9eZYcPZia7CtZD4IUH5GIUPS8bDaTdCXZ1GxS6X9vtLXUuczA_Pjm8SF0HgazEHMmru-e54tZLAQn_AiNQ0FDnwlMjg_qEZo69xEMwTGPMDlFIxxRGuAoGqMksR24zlhVeemmXi2VLQ3oTjmjbrzEOlMuO-c11ntRVpVQg-08ZXMvNR20qutb8BawNvB1hk4KVTmY7vIEvT_cv82f_PT1MZnfpb4mMe18neEsiwRgiguNtRYFBx1rxgpF8ijDQEiOscZUiwwHLAZgGVExj4uQ4UAUZIJut7qrPqsh18NCrarkqjW1ajeyUUb-71izlGWzllSwiJNgELjcCbTNZz8cL2vjNFSVstD0ToZxwCllLCIDerVFdds410KxHxMG8tcA-WOA3Bow4BeHq-3hv3eTbxAXgpc</recordid><startdate>20160721</startdate><enddate>20160721</enddate><creator>Alshikho, Mohamad J</creator><creator>Talas, Joud M</creator><creator>Noureldine, Salem I</creator><creator>Zazou, Saf</creator><creator>Addas, Aladdin</creator><creator>Kurabi, Haitham</creator><creator>Nasser, Mahmoud</creator><general>International Scientific Literature, 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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160721</creationdate><title>Intestinal Lymphangiectasia: Insights on Management and Literature Review</title><author>Alshikho, Mohamad J ; Talas, Joud M ; Noureldine, Salem I ; Zazou, Saf ; Addas, Aladdin ; Kurabi, Haitham ; Nasser, Mahmoud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-cb2bb79e242fc2cc9f6ec8c55fa3d7b2e33d22c24c9b2058ee5b3a868f15209f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biopsy</topic><topic>Diagnosis, Differential</topic><topic>Diarrhea - diagnosis</topic><topic>Diarrhea - etiology</topic><topic>Diarrhea - therapy</topic><topic>Disease Management</topic><topic>Endoscopy, Digestive System</topic><topic>Humans</topic><topic>Intestines - diagnostic imaging</topic><topic>Lymphangiectasis, Intestinal - complications</topic><topic>Lymphangiectasis, Intestinal - diagnosis</topic><topic>Lymphangiectasis, Intestinal - therapy</topic><topic>Male</topic><topic>Radiography, Abdominal</topic><topic>Tomography, X-Ray Computed</topic><topic>Ultrasonography</topic><topic>Young Adult</topic><toplevel>online_resources</toplevel><creatorcontrib>Alshikho, Mohamad J</creatorcontrib><creatorcontrib>Talas, Joud M</creatorcontrib><creatorcontrib>Noureldine, Salem I</creatorcontrib><creatorcontrib>Zazou, Saf</creatorcontrib><creatorcontrib>Addas, Aladdin</creatorcontrib><creatorcontrib>Kurabi, Haitham</creatorcontrib><creatorcontrib>Nasser, Mahmoud</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alshikho, Mohamad J</au><au>Talas, Joud M</au><au>Noureldine, Salem I</au><au>Zazou, Saf</au><au>Addas, Aladdin</au><au>Kurabi, Haitham</au><au>Nasser, Mahmoud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intestinal Lymphangiectasia: Insights on Management and Literature Review</atitle><jtitle>The American journal of case reports</jtitle><addtitle>Am J Case Rep</addtitle><date>2016-07-21</date><risdate>2016</risdate><volume>17</volume><spage>512</spage><epage>522</epage><pages>512-522</pages><issn>1941-5923</issn><eissn>1941-5923</eissn><abstract>BACKGROUND Intestinal lymphangiectasia (IL) is a rare disease characterized by a dilatation of the intestinal lymphatics and loss of lymph fluid into the gastrointestinal tract leading to hypoproteinemia, edema, lymphocytopenia, hypogammaglobinemia, and immunological abnormalities. Iron, calcium, and other serum components (e.g., lipids, fat soluble vitamins) may also be depleted. A literature search revealed more than 200 reported cases of IL. Herein, we report our observations of a patient diagnosed with IL; we also present our conclusion for our review of the published literature. CASE REPORT A 24-year-old male was admitted to Aleppo University Hospital with the complaints of abdominal pain, headache, arthralgia, fever, and rigors. His past medical history was remarkable for frequent episodes of diarrhea, recurrent infections, and swelling in the lower limbs. In addition, he had been hospitalized several times in non-academic hospitals due to edema in his legs, cellulitis, and recurrent infections. In the emergency department, a physical examination revealed a patient in distress. He was weak, dehydrated, pale, and had a high-grade fever. His lower extremities were edematous, swollen, and extremely tender to touch. The overlying skin was erythematous and warm. Moreover, the patient was tachycardic, tacypneic, and moderately hypotensive. The patient was resuscitated with IV fluids, and Tylenol was administered to bring the temperature down. Blood tests showed anemia and high levels of inflammatory markers. The patient's white blood cell count was elevated with an obvious left shift. However, subsequent investigations showed that the patient had IL. Suitable diet modification plans were applied as a long-term management plan. CONCLUSIONS IL is a rare disease of challenging nature due to its systematic effects and lack of comprehensive studies that can evaluate the effectiveness of specific treatments in a large cohort of patients. MCT (medium-chain triglyceride) oils and diet modification strategies are effective in reducing the loss of body proteins and in maintaining near-normal blood levels of immunoglobulins. However, octreotide and MCT oils had no proven role in shrinking edema in our patient.</abstract><cop>United States</cop><pub>International Scientific Literature, Inc</pub><pmid>27440277</pmid><doi>10.12659/AJCR.899636</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1941-5923
ispartof The American journal of case reports, 2016-07, Vol.17, p.512-522
issn 1941-5923
1941-5923
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4957630
source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
subjects Biopsy
Diagnosis, Differential
Diarrhea - diagnosis
Diarrhea - etiology
Diarrhea - therapy
Disease Management
Endoscopy, Digestive System
Humans
Intestines - diagnostic imaging
Lymphangiectasis, Intestinal - complications
Lymphangiectasis, Intestinal - diagnosis
Lymphangiectasis, Intestinal - therapy
Male
Radiography, Abdominal
Tomography, X-Ray Computed
Ultrasonography
Young Adult
title Intestinal Lymphangiectasia: Insights on Management and Literature Review
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T08%3A58%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intestinal%20Lymphangiectasia:%20Insights%20on%20Management%20and%20Literature%20Review&rft.jtitle=The%20American%20journal%20of%20case%20reports&rft.au=Alshikho,%20Mohamad%20J&rft.date=2016-07-21&rft.volume=17&rft.spage=512&rft.epage=522&rft.pages=512-522&rft.issn=1941-5923&rft.eissn=1941-5923&rft_id=info:doi/10.12659/AJCR.899636&rft_dat=%3Cproquest_pubme%3E1806445573%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1806445573&rft_id=info:pmid/27440277&rfr_iscdi=true