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The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin
Pseudomyxoma peritonei (PMP) is a rare clinical entity characterized by widespread mucinous implants in the peritoneal cavity. Commonly seen in females in their 50s, PMP typically originates from ruptured appendiceal mucoceles that find refuge in the peritoneal space. Rarely, PMP may originate from...
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Published in: | JIM - high impact case reports 2023-01, Vol.11, p.23247096231217822-23247096231217822 |
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description | Pseudomyxoma peritonei (PMP) is a rare clinical entity characterized by widespread mucinous implants in the peritoneal cavity. Commonly seen in females in their 50s, PMP typically originates from ruptured appendiceal mucoceles that find refuge in the peritoneal space. Rarely, PMP may originate from the ovary, stomach, colon, or pancreas. Pseudomyxoma peritonei of colorectal origin is more malignant and has a lower survival rate. We report a case of a 59-year-old Hispanic woman with PMP who presented to the emergency room with a 3-month history of progressive abdominal distention. Pseudomyxoma peritonei was confirmed by computed tomography (CT) scan of the abdomen and pelvis and histopathology, and the patient underwent partial cytoreductive surgery. Given her Eastern Cooperative Oncology Group (ECOG) performance status of 1 despite extensive carcinomatosis, our patient may benefit from hyperthermic intraperitoneal chemotherapy (HIPEC) in the future. |
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Commonly seen in females in their 50s, PMP typically originates from ruptured appendiceal mucoceles that find refuge in the peritoneal space. Rarely, PMP may originate from the ovary, stomach, colon, or pancreas. Pseudomyxoma peritonei of colorectal origin is more malignant and has a lower survival rate. We report a case of a 59-year-old Hispanic woman with PMP who presented to the emergency room with a 3-month history of progressive abdominal distention. Pseudomyxoma peritonei was confirmed by computed tomography (CT) scan of the abdomen and pelvis and histopathology, and the patient underwent partial cytoreductive surgery. Given her Eastern Cooperative Oncology Group (ECOG) performance status of 1 despite extensive carcinomatosis, our patient may benefit from hyperthermic intraperitoneal chemotherapy (HIPEC) in the future.</description><identifier>ISSN: 2324-7096</identifier><identifier>EISSN: 2324-7096</identifier><identifier>DOI: 10.1177/23247096231217822</identifier><identifier>PMID: 38102072</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Abdomen ; Appendiceal Neoplasms - complications ; Appendiceal Neoplasms - pathology ; Cancer ; Cancer surgery ; Case reports ; Female ; Humans ; Middle Aged ; Mucocele - complications ; Mucocele - pathology ; Peritoneal Neoplasms - diagnosis ; Peritoneal Neoplasms - therapy ; Pseudomyxoma Peritonei - diagnosis ; Pseudomyxoma Peritonei - drug therapy ; Pseudomyxoma Peritonei - etiology ; Pseudomyxoma Peritonei - pathology</subject><ispartof>JIM - high impact case reports, 2023-01, Vol.11, p.23247096231217822-23247096231217822</ispartof><rights>2023 American Federation for Medical Research</rights><rights>2023 American Federation for Medical Research. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c429t-55225891ddfed1b41117d8f5ae4feef7d3b99b697ed505b7a1b9a38564a50db23</cites><orcidid>0000-0002-2772-6085</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/23247096231217822$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2920173175?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,21966,25753,27853,27924,27925,37012,37013,44590,44945,45333</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38102072$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bathobakae, Lefika</creatorcontrib><creatorcontrib>Ozgur, Sacide S.</creatorcontrib><creatorcontrib>Jariwala, Mohita</creatorcontrib><creatorcontrib>Kesrani, Jaydev</creatorcontrib><creatorcontrib>Ajas, Shajla</creatorcontrib><creatorcontrib>Kumar, Mehandar</creatorcontrib><creatorcontrib>Akmal, Amer</creatorcontrib><title>The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin</title><title>JIM - high impact case reports</title><addtitle>J Investig Med High Impact Case Rep</addtitle><description>Pseudomyxoma peritonei (PMP) is a rare clinical entity characterized by widespread mucinous implants in the peritoneal cavity. Commonly seen in females in their 50s, PMP typically originates from ruptured appendiceal mucoceles that find refuge in the peritoneal space. Rarely, PMP may originate from the ovary, stomach, colon, or pancreas. Pseudomyxoma peritonei of colorectal origin is more malignant and has a lower survival rate. We report a case of a 59-year-old Hispanic woman with PMP who presented to the emergency room with a 3-month history of progressive abdominal distention. Pseudomyxoma peritonei was confirmed by computed tomography (CT) scan of the abdomen and pelvis and histopathology, and the patient underwent partial cytoreductive surgery. Given her Eastern Cooperative Oncology Group (ECOG) performance status of 1 despite extensive carcinomatosis, our patient may benefit from hyperthermic intraperitoneal chemotherapy (HIPEC) in the future.</description><subject>Abdomen</subject><subject>Appendiceal Neoplasms - complications</subject><subject>Appendiceal Neoplasms - pathology</subject><subject>Cancer</subject><subject>Cancer surgery</subject><subject>Case reports</subject><subject>Female</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>Mucocele - complications</subject><subject>Mucocele - pathology</subject><subject>Peritoneal Neoplasms - diagnosis</subject><subject>Peritoneal Neoplasms - therapy</subject><subject>Pseudomyxoma Peritonei - diagnosis</subject><subject>Pseudomyxoma Peritonei - drug therapy</subject><subject>Pseudomyxoma Peritonei - etiology</subject><subject>Pseudomyxoma Peritonei - pathology</subject><issn>2324-7096</issn><issn>2324-7096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kV9vFCEUxYnR2Kb2A_hiJvHFl63ADAP4tln_tEmTbkx9Jhe4s7KZGUbYSey3l-nW1mjkBXL4nQM3h5DXjF4wJuV7XvNGUt3ymnEmFefPyOmirRbx-R_nE3Ke856WpUQh9UtyUitGOZX8lGxvv2O1gdFhqj4GyFNM8KFaV18hLXrGKnbVNuPs43D3Mw5QbTGFQxwxLDfracLRB4fQVzcp7ML4irzooM94_rCfkW-fP91uLlfXN1-uNuvrlWu4PqyE4Fwozbzv0DPbsDKTV50AbDrETvraam1bLdELKqwEZjXUSrQNCOotr8_I1THXR9ibKYUB0p2JEMy9ENPOQDoE16OpqbMcHFUtQMM8140TFjslZYuILZasd8esKcUfM-aDGUJ22PcwYpyz4ZoWkxJSFPTtX-g-zmkskxaKUyZrdk-xI-VSzDlh9_hBRs3SnvmnveJ585A82wH9o-N3VwW4OAIZdvj07P8TfwGQhJ8s</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Bathobakae, Lefika</creator><creator>Ozgur, Sacide S.</creator><creator>Jariwala, Mohita</creator><creator>Kesrani, Jaydev</creator><creator>Ajas, Shajla</creator><creator>Kumar, Mehandar</creator><creator>Akmal, Amer</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><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>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>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2772-6085</orcidid></search><sort><creationdate>20230101</creationdate><title>The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin</title><author>Bathobakae, Lefika ; 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Commonly seen in females in their 50s, PMP typically originates from ruptured appendiceal mucoceles that find refuge in the peritoneal space. Rarely, PMP may originate from the ovary, stomach, colon, or pancreas. Pseudomyxoma peritonei of colorectal origin is more malignant and has a lower survival rate. We report a case of a 59-year-old Hispanic woman with PMP who presented to the emergency room with a 3-month history of progressive abdominal distention. Pseudomyxoma peritonei was confirmed by computed tomography (CT) scan of the abdomen and pelvis and histopathology, and the patient underwent partial cytoreductive surgery. Given her Eastern Cooperative Oncology Group (ECOG) performance status of 1 despite extensive carcinomatosis, our patient may benefit from hyperthermic intraperitoneal chemotherapy (HIPEC) in the future.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>38102072</pmid><doi>10.1177/23247096231217822</doi><orcidid>https://orcid.org/0000-0002-2772-6085</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Appendiceal Neoplasms - complications Appendiceal Neoplasms - pathology Cancer Cancer surgery Case reports Female Humans Middle Aged Mucocele - complications Mucocele - pathology Peritoneal Neoplasms - diagnosis Peritoneal Neoplasms - therapy Pseudomyxoma Peritonei - diagnosis Pseudomyxoma Peritonei - drug therapy Pseudomyxoma Peritonei - etiology Pseudomyxoma Peritonei - pathology |
title | The Cancer Diaspora: A Rare Case of Pseudomyxoma Peritonei of Appendiceal Origin |
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