Literature DB >> 11454998

Gelatinous ascites: a cytohistologic study of pseudomyxoma peritonei in 67 patients.

S L Jackson1, R A Fleming, B W Loggie, K R Geisinger.   

Abstract

BACKGROUND: Pseudomyxoma peritonei (PMP) is a rare condition characterized by gelatinous ascites. Although the histologic attributes of PMP have been well studied, the cytologic features remain ill defined.
METHODS: We reviewed the peritoneal washings (PW) in 67 patients with PMP to identify cytomorphologic features useful in classifying cases as either disseminated peritoneal adenomucinosis (DPAM) or peritoneal mucinous carcinomatosis (PMCA). Histologic specimens were correlated with the cytologic diagnoses. Correlation between cytologic diagnosis and patient outcome was investigated.
RESULTS: Neoplastic epithelial cells were identified in 63 of 67 PW (94%). Concordance with the histologic diagnosis was obtained in 61 of 63 cases. Of these 36.5% were cytologically classified as DPAM with primary appendiceal neoplasms in 19 cases. Thirty-four of 63 cases (53.9%) were cytologically diagnosed as PMCA based on PW cytology. Most were of appendiceal or colonic origin. Four cases displayed cytologic features of both DPAM and PMCA. Two discordant cases each with a cytologic diagnosis of PMCA had an appendiceal adenoma. Acellular mucin alone was identified in the PW in four cases. Analysis of follow-up data revealed that cases diagnosed as DPAM had a better prognosis than those diagnosed as PMCA.
CONCLUSIONS: Cytomorphologic features of epithelial cells in PW material can accurately categorize cases of PMP as either DPAM or PMCA. Furthermore, this categorization appears to have important prognostic implications.

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Year:  2001        PMID: 11454998     DOI: 10.1038/modpathol.3880370

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  9 in total

1.  Pseudomyxoma peritonei originating from urachus-case report and review of the literature.

Authors:  A K Agrawal; P Bobiński; Z Grzebieniak; J Rudnicki; G Marek; P Kobielak; M Kazanowski; S Agrawal; A Hałoń
Journal:  Curr Oncol       Date:  2014-02       Impact factor: 3.677

2.  Rare Presentation of Pseudomyxoma Retroperitonei: Stretching the Limits.

Authors:  Roumina Hasan; Sandeep Kumar; Anuradha Ck Rao; Rajagopal Kadavigere
Journal:  Malays J Med Sci       Date:  2016-06-30

3.  Pseudomyxoma peritonei is a disease of MUC2-expressing goblet cells.

Authors:  Jerome T O'Connell; James S Tomlinson; Alice A Roberts; Kathryn F McGonigle; Sanford H Barsky
Journal:  Am J Pathol       Date:  2002-08       Impact factor: 4.307

4.  Pseudomyxoma peritonei: a rare presentation as an umbilical nodule.

Authors:  N Srinivasaiah; G Retnasingam; R Kasarneni; B Slater
Journal:  Ir J Med Sci       Date:  2008-01-26       Impact factor: 1.568

Review 5.  Appendiceal Neoplasms.

Authors:  Quinton M Hatch; Erin W Gilbert
Journal:  Clin Colon Rectal Surg       Date:  2018-09-04

6.  Pseudomyxoma peritonei of 92 Chinese patients: clinical characteristics, pathological classification and prognostic factors.

Authors:  Ai-Tao Guo; Yan-Mi Li; Li-Xin Wei
Journal:  World J Gastroenterol       Date:  2012-06-28       Impact factor: 5.742

7.  Updated staging and patient outcomes in low-grade appendiceal mucinous neoplasms.

Authors:  Samuel J Ballentine; Jacquelyn Carr; Eliahu Y Bekhor; Umut Sarpel; Alexandros D Polydorides
Journal:  Mod Pathol       Date:  2020-07-29       Impact factor: 7.842

8.  Abdominopelvic washings: A comprehensive review.

Authors:  Erika F Rodriguez; Sara E Monaco; Walid Khalbuss; R Marshall Austin; Liron Pantanowitz
Journal:  Cytojournal       Date:  2013-04-24       Impact factor: 2.091

Review 9.  Comprehensive Understanding and Evolutional Therapeutic Schemes for Pseudomyxoma Peritonei: A Literature Review.

Authors:  Suiting Ye; Song Zheng
Journal:  Am J Clin Oncol       Date:  2022-04-14       Impact factor: 2.787

  9 in total

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