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 : 2975

Journal of Clinical & Experimental Pathology received 2975 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

Title: The synchronous gastrointestinal neuroendocrine tumors, colorectal adenocarcinoma and liver cavernous hemangioma-histopathological, immunohistochemical and genetic case report study

20th European Pathology Congress

Liga Sulca, Selga Savcenko, Viktorija Kregere

Riga East University Hospital, Latvia

Posters & Accepted Abstracts: J Clin Exp Pathol

Abstract
The incidence of synchronous gastrointestinal neuroendocrine tumors (NET) and colorectal cancer is very low (Yumoto S, 2020). NET are relatively rare tumors and located most commonly in the gastrointestinal tract mainly in small intestine and rectum. Generally, NETs often show hematogenous metastases, and the most frequent site of distant spread is liver (Yumoto S, 2020). Colorectal carcinoma is one of common malignant tumor. The adenocarcinoma is the frequent histopathological tumor type. (Yumoto S, 2020). The synchronous tumors usually are inherited and are related with multiple endocrine neoplasia syndrome (Yumoto S, 2020). We report the case of a 70-year-old male with multiple sinchronous tumours- primary small intestinal neuroendocrine tumor, colorectal carcinoma and liver cavernous hemangioma. A 70 years old male was addmitted at Pauls Stradins Clinical University Hospital with previously biopsy proved Grade 2 colorectal carcinoma for surgical treatment. Clinical examination was performed. CT scanning showed suspicious liver mass, probably metastasis. In addition, in small intestine mass lesions were observed. The surgical treatment was performed. The histopathological, immunohistochemical and genetic examination was performed. The comprehensive next generation sequencing was performed (Quigen). Such genes were analyzed-APC, AKT2, AKT3, AR, ARAF, ARID1A, BAP1, BRCA1, BRCA2, BRAF, CDH1, CDK4, CSF1R, CDKN, CTCF, ERBB3, ESR1, FAT1, FOXL2, GATA3, GNA11, GNAQ, H3F3A, HIST1H3 B, HNF1A, HRAS, IDH1, IDH2, JAK2, KDR, KRAS, KEAP1, KMT2C, KMT2D, MAP2K2, MLH1, NF1, NFE2L2, PDGFRA, PIK3R1, POLE, RAC1, RB1, RHOA, SF3B1, SMARCB 1, SRC, TSC1, TSC2, U2AF1, VHL. Histopathological examination demonstrated multiple sinchronous tumors. The patients has liver cavernous hemangioma, muliple small intestinal neuroendocrine tumor Grade 2 (NET Grade 2) measured 0.4 cm �¸ and 0,6 cm �¸ , pT3(m)N0M0 and Grade 3 colorectal adenocarcinoma, pT2N1cM0. Immunohistochemical examination confirmed NET diagnosis, the tumor was positive for chromogranene and synaptophysine, Ki-67 index was 5%. The Grade 3 colorectal adenocarcinoma was positive for CKAE1/AE3. Obtained results showed that small intestine NET had CDKN1B, DAXX and ATRX mutations, however MLH1, MSH2, MSH6, PMS2 mutations have not been observed. Colorectal adenocarcinoma had p53, SMAD4, PIK3CA and BRAF mutations, however MLH1, MSH2, MSH6, PMS2 and KRAS mutations have not been identified. To conclude, our case report rare coexistent synchronous tumors-liver cavernous hemangioma, small intestinal neuroendocrine tumors and colorectal adenocarcinoma. Based on NGS analysis small intestinal NET more likely corresponded to MEN 4 syndrome, however the genetical mutations of colorectal carcinoma demonstrated MSI wild type tumour which did not fulfill with MEN syndrome. This case emphasizes that for synchronous cancer the surgical resection and hitopathological examination is requiered before systemic therapy regardless of the difference in prognosis between the synchronous tumors.
Biography

Liga Sulca, MD, graduated from Faculty of Medicine, University of Latvia in 2020. Currently she is a 2 year resident at Riga East University Hospital, Centre of Pathology and University of Latvia. Interested in gastrointestinal pathology, renal pathology and neuropathology. Participated in different local and international scientific conferences. Viktorija Kregere, MD. graduated from Faculty of Medicine, University of Latvia in 2017. Currently she is a 4 year resident at Riga East University Hospital, Centre of Pathology and University of Latvia. Interested in bone and soft tissue, prostate pathology and molecular pathology. Participated in different local and international scientific conferences. Selga Savcenko, MD graduated from Faculty of Medicine, University of Latvia in 2017. She was a founder of student scientific pathology group at Faculty of Medicine, University of Latvia and its chair till 2017. Currently she is a 4 year resident at Riga East University Hospital, Centre of Pathology and University of Latvia. Interested in gynecological, gastrointestinal, breast and molecular pathology. Participated in different local and international scientific conferences. She published two PubMed peer reviewed publications in journals Virchows Archiv and Diagnostics.

Top