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A Diagnostic Challenge: A Case of Disseminated Nocardiosis Presenting With Generalized Lymphadenopathy in a Patient With Interleukin-12 Deficiency
Deficiency in interleukin-12 (IL-12) can result in susceptibility to opportunistic infection, with IL-12 deficiency being a rare genetic cause. is a gram-positive aerobic actinomycete that can cause disseminated and potentially lethal nocardiosis in immunocompromised patients. This report describes...
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Published in: | Curēus (Palo Alto, CA) CA), 2024-06, Vol.16 (6), p.e62396 |
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description | Deficiency in interleukin-12 (IL-12) can result in susceptibility to opportunistic infection, with IL-12 deficiency being a rare genetic cause.
is a gram-positive aerobic actinomycete that can cause disseminated and potentially lethal nocardiosis in immunocompromised patients. This report describes a 16-year-old male adolescent with IL-12 deficiency presenting with generalized lymphadenopathy due to disseminated
The subject of our study is a male adolescent who exhibited clinical manifestations consistent with cholestasis. He underwent extensive workup for malignancy, suspecting cholangiocarcinoma initially. The workup turned out unremarkable, and later during his hospital stay, he deteriorated and required intensive care unit (ICU) admission, as he developed superior vena cava (SVC) syndrome from massive enlargement of mediastinal and cervical lymph nodes. During the patient's admission, it was found that he had a deficiency of interleukin-12 (IL-12). Later on, a blood culture revealed the presence of
species. Subsequently, the patient was initiated and improved drastically on an empirical antibiotic regimen consisting of amikacin, co-trimoxazole, meropenem, and moxifloxacin. Following that, the susceptibility results came out, and he was switched to oral co-trimoxazole and oral moxifloxacin as he no longer required inpatient care. This report highlights the importance of accurate diagnosis of causes of immunosuppression and early investigation, diagnosis, and management of potentially fatal opportunistic infections such as disseminated |
doi_str_mv | 10.7759/cureus.62396 |
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is a gram-positive aerobic actinomycete that can cause disseminated and potentially lethal nocardiosis in immunocompromised patients. This report describes a 16-year-old male adolescent with IL-12 deficiency presenting with generalized lymphadenopathy due to disseminated
The subject of our study is a male adolescent who exhibited clinical manifestations consistent with cholestasis. He underwent extensive workup for malignancy, suspecting cholangiocarcinoma initially. The workup turned out unremarkable, and later during his hospital stay, he deteriorated and required intensive care unit (ICU) admission, as he developed superior vena cava (SVC) syndrome from massive enlargement of mediastinal and cervical lymph nodes. During the patient's admission, it was found that he had a deficiency of interleukin-12 (IL-12). Later on, a blood culture revealed the presence of
species. Subsequently, the patient was initiated and improved drastically on an empirical antibiotic regimen consisting of amikacin, co-trimoxazole, meropenem, and moxifloxacin. Following that, the susceptibility results came out, and he was switched to oral co-trimoxazole and oral moxifloxacin as he no longer required inpatient care. This report highlights the importance of accurate diagnosis of causes of immunosuppression and early investigation, diagnosis, and management of potentially fatal opportunistic infections such as disseminated</description><identifier>ISSN: 2168-8184</identifier><identifier>EISSN: 2168-8184</identifier><identifier>DOI: 10.7759/cureus.62396</identifier><identifier>PMID: 39006736</identifier><language>eng</language><publisher>United States: Cureus Inc</publisher><subject>Abdomen ; Abscesses ; Biopsy ; Bone marrow ; Cytokines ; Endoscopy ; Hemodynamics ; Infections ; Infectious Disease ; Intensive care ; Lymphatic system ; Medical diagnosis ; Medical imaging ; Pleural effusion ; Teenagers ; Tomography ; Urine</subject><ispartof>Curēus (Palo Alto, CA), 2024-06, Vol.16 (6), p.e62396</ispartof><rights>Copyright © 2024, Mitwalli et al.</rights><rights>Copyright © 2024, Mitwalli et al. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2024, Mitwalli et al. 2024 Mitwalli et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c300t-1396b8c567252d276ac24132386492cc5b441a971eeeaaa73c6fa15fb9b6191e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3086750549/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3086750549?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39006736$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitwalli, Hussam</creatorcontrib><creatorcontrib>Alekrish, Yazeed</creatorcontrib><creatorcontrib>Nafisah, Faris</creatorcontrib><creatorcontrib>Alkhamshi, Abdullah</creatorcontrib><title>A Diagnostic Challenge: A Case of Disseminated Nocardiosis Presenting With Generalized Lymphadenopathy in a Patient With Interleukin-12 Deficiency</title><title>Curēus (Palo Alto, CA)</title><addtitle>Cureus</addtitle><description>Deficiency in interleukin-12 (IL-12) can result in susceptibility to opportunistic infection, with IL-12 deficiency being a rare genetic cause.
is a gram-positive aerobic actinomycete that can cause disseminated and potentially lethal nocardiosis in immunocompromised patients. This report describes a 16-year-old male adolescent with IL-12 deficiency presenting with generalized lymphadenopathy due to disseminated
The subject of our study is a male adolescent who exhibited clinical manifestations consistent with cholestasis. He underwent extensive workup for malignancy, suspecting cholangiocarcinoma initially. The workup turned out unremarkable, and later during his hospital stay, he deteriorated and required intensive care unit (ICU) admission, as he developed superior vena cava (SVC) syndrome from massive enlargement of mediastinal and cervical lymph nodes. During the patient's admission, it was found that he had a deficiency of interleukin-12 (IL-12). Later on, a blood culture revealed the presence of
species. Subsequently, the patient was initiated and improved drastically on an empirical antibiotic regimen consisting of amikacin, co-trimoxazole, meropenem, and moxifloxacin. Following that, the susceptibility results came out, and he was switched to oral co-trimoxazole and oral moxifloxacin as he no longer required inpatient care. This report highlights the importance of accurate diagnosis of causes of immunosuppression and early investigation, diagnosis, and management of potentially fatal opportunistic infections such as disseminated</description><subject>Abdomen</subject><subject>Abscesses</subject><subject>Biopsy</subject><subject>Bone marrow</subject><subject>Cytokines</subject><subject>Endoscopy</subject><subject>Hemodynamics</subject><subject>Infections</subject><subject>Infectious Disease</subject><subject>Intensive care</subject><subject>Lymphatic system</subject><subject>Medical diagnosis</subject><subject>Medical imaging</subject><subject>Pleural effusion</subject><subject>Teenagers</subject><subject>Tomography</subject><subject>Urine</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkU1v1DAYhC0EotXSG2dkiQsHUvyR2AkXtNpCqbSCHkAcrTfOm41L1t7aCdLyM_qL67KlKpxsaR6PZjyEvOTsVOuqeWfniHM6VUI26gk5FlzVRc3r8umj-xE5SemKMcaZFkyz5-RINowpLdUxuVnSMwcbH9LkLF0NMI7oN_ieLukKEtLQZz0l3DoPE3b0S7AQOxeSS_QyYkI_Ob-hP9w00HP0GGF0vzO33m93A3Toww6mYU-dp0AvYXL5wYG-8BPGEeefzhdc0DPsnc2q3b8gz3oYE57cnwvy_dPHb6vPxfrr-cVquS6sZGwqeK7c1rZSWlSiE1qBFSWXQtaqbIS1VVuWHBrNEREAtLSqB171bdMq3nCUC_Lh4Lub2y12NifL6c0uui3EvQngzL-Kd4PZhF-Gc1Hm32PZ4c29QwzXM6bJbF2yOI7gMczJSFYzJVWV51mQ1_-hV2GOPve7o5SuWFU2mXp7oGwMKUXsH9JwZu4GN4fBzZ_BM_7qcYMH-O-88hZhGqki</recordid><startdate>20240614</startdate><enddate>20240614</enddate><creator>Mitwalli, Hussam</creator><creator>Alekrish, Yazeed</creator><creator>Nafisah, Faris</creator><creator>Alkhamshi, Abdullah</creator><general>Cureus Inc</general><general>Cureus</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240614</creationdate><title>A Diagnostic Challenge: A Case of Disseminated Nocardiosis Presenting With Generalized Lymphadenopathy in a Patient With Interleukin-12 Deficiency</title><author>Mitwalli, Hussam ; 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is a gram-positive aerobic actinomycete that can cause disseminated and potentially lethal nocardiosis in immunocompromised patients. This report describes a 16-year-old male adolescent with IL-12 deficiency presenting with generalized lymphadenopathy due to disseminated
The subject of our study is a male adolescent who exhibited clinical manifestations consistent with cholestasis. He underwent extensive workup for malignancy, suspecting cholangiocarcinoma initially. The workup turned out unremarkable, and later during his hospital stay, he deteriorated and required intensive care unit (ICU) admission, as he developed superior vena cava (SVC) syndrome from massive enlargement of mediastinal and cervical lymph nodes. During the patient's admission, it was found that he had a deficiency of interleukin-12 (IL-12). Later on, a blood culture revealed the presence of
species. Subsequently, the patient was initiated and improved drastically on an empirical antibiotic regimen consisting of amikacin, co-trimoxazole, meropenem, and moxifloxacin. Following that, the susceptibility results came out, and he was switched to oral co-trimoxazole and oral moxifloxacin as he no longer required inpatient care. This report highlights the importance of accurate diagnosis of causes of immunosuppression and early investigation, diagnosis, and management of potentially fatal opportunistic infections such as disseminated</abstract><cop>United States</cop><pub>Cureus Inc</pub><pmid>39006736</pmid><doi>10.7759/cureus.62396</doi><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Abscesses Biopsy Bone marrow Cytokines Endoscopy Hemodynamics Infections Infectious Disease Intensive care Lymphatic system Medical diagnosis Medical imaging Pleural effusion Teenagers Tomography Urine |
title | A Diagnostic Challenge: A Case of Disseminated Nocardiosis Presenting With Generalized Lymphadenopathy in a Patient With Interleukin-12 Deficiency |
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