ISSN: 2161-0681

Journal of Clinical & Experimental Pathology
Open Access

Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
Google Scholar citation report
Citations : 1437

Journal of Clinical & Experimental Pathology received 1437 citations as per Google Scholar report

Journal of Clinical & Experimental Pathology peer review process verified at publons
Indexed In
  • Index Copernicus
  • Google Scholar
  • Sherpa Romeo
  • Open J Gate
  • Genamics JournalSeek
  • JournalTOCs
  • Cosmos IF
  • Ulrich's Periodicals Directory
  • RefSeek
  • Directory of Research Journal Indexing (DRJI)
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • Publons
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • ICMJE
  • world cat
  • journal seek genamics
  • j-gate
  • esji (eurasian scientific journal index)
Share This Page

Concurrent splenic lymphangiomatosis and proteus syndrome

3rd International Conference and Exhibition on Pathology

Reja Syed Emran

ScientificTracks Abstracts: J Clin Exp Pathol

DOI: 10.4172/2161-0681.S1.012

Abstract
A37-year-old female presented with Proteus syndrome and was found to have an asymptomatic enlarged spleen. Pathology confirmed splenic lymphangiomatosis. Proteus syndrome is a rare congenital disorder. It was named after the Greek god Proteus, meaning ?The Polymorphous?, for he could avoid capture by altering his shape. It can manifest usually as progressive skeletal abnormalities including asymmetric overgrowth, macrodactyly, scoliosis, and limb length discrepancy followed by soft tissue anomalies namely fatty, muscular, lymphatic and vascular malformations. Visceral malformations are rare including splenomegaly. In this case report, we highlight the rare association of this syndrome with lymphangiomatosis in the Middle- Eastern population.
Biography
Reja Syed Emran completed her Bachelors of Medicine and Surgery (MBBS) Degree from Army medical College, Pakistan at the age of 23 and is currently residing in Saudi Arabia, and an intern at King Faisal Specialist Hospital & Research Center, Riyadh. She has participated and assisted in research projects, and published a case report with her colleagues while rotating in the Department of General Surgery.
Top