<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/css" href="https://imcjms.com/public/assets/rss.css" ?><rss version="2.0">
<channel>
    <title>IMC Journal of Medical Science</title>
    <link>https://imcjms.com/public</link>
    <description>Ibrahim Medical College Journal of Medical Science</description>

                        <item>
                <title><![CDATA[Clinicopathologic features, management and outcome of ten cases of gastrointestinal stromal tumors]]></title>

                                    <author><![CDATA[Md. Nazmul Hoque]]></author>
                                    <author><![CDATA[Samiron Kumar Mondal]]></author>
                                    <author><![CDATA[Md. Mohsin Kabir]]></author>
                                    <author><![CDATA[Indrejit Kumar Datta]]></author>
                                    <author><![CDATA[M Golam Azam]]></author>
                                    <author><![CDATA[Md. Abdullah Al Mamoon]]></author>
                                    <author><![CDATA[Shireen Ahmed]]></author>
                
                <link data-url="https://imcjms.com/public/registration/journal_full_text/201">
    https://imcjms.com/public/registration/journal_full_text/201
</link>
                <pubDate>Sat, 22 Apr 2017 10:43:32 +0000</pubDate>
                <category><![CDATA[Original Article]]></category>
                <comments><![CDATA[IMC J Med Sci 2017; 11(2): 45-49]]></comments>
                <description>Abstract
Background and
objectives:Gastrointestinal stromal tumor (GISTs) is an uncommon and rare
disease in Bangladesh. Our aims were to describe
socio-demographic characteristics, clinical presentations, anatomical location,
morphological variation, treatment and outcome of GIST in ten cases.
Methods:This study included consecutive ten cases of GISTs diagnosed
and treated in two tertiary level hospitals in Dhaka, Bangladesh from 2013 to
2016. Patients’ socio-demographic characteristics, clinical presentations,
anatomical location, histological types, presence of CD117 markers were
determined. Outcome of the treatment by surgical intervention and imatinib mesylate
(400mg/day) were evalauted. 
Results: Total 10 patients were included in the study. Among them 6 were
male and 4 were female. The age range was 32-74 years. Abdominal pain, haematemesis,
melaena, haematochezia and anaemia
were the most common presentation. One patient had dysphagia and another had
features of subacute intestinal obstruction. Five patients had GIST in the
stomach (50%), two had in colon and one in esophagus, duodenum and ileum
respectively. CD 117 was positive in 8 cases, majority had spindly type cell
with low mitotic figure. Imatinib therapy was given in all the cases except two
patients. Disease recurrence in the form liver metastasis was found in two
cases and both died. Disease free survival for more than 2 years was observed
in 4 cases. 
Conclusion: Haematemesis and melaena were common presentation of GISTs.
Stomach was the most common site for GISTs and majority had spindle type of
cells and positive CD117 marker. Surgical intervention and imatinib therapy was
found effective.
IMC J Med
Sci 2017; 11(2): 45-49.&amp;nbsp;DOI: https://doi.org/10.3329/imcjms.v11i2.33094    
Address for Correspondence: Dr. Md. Nazmul Hoque,
Consultant and Head, Department of GHPD, Ibrahim Medical College &amp;amp; BIRDEM
General Hospital, 122 Kazi Nazrul Islam Avenue, Dhaka, Bangladesh. Email: alifbd@gmail.com
&amp;nbsp;
Introduction
Gastrointestinal
stromal tumors (GISTs) are the mesenchymal tumors of the gastrointestinal tract
(GI) and account for less than 1% of GI
tumors [1]. About 60%-70% GIST arises
from the stomach and the rest are from small
intestine (20% to 30%), colon and rectum (5%), and esophagus (&amp;lt;5%) [2].
A small number of stromal tumors may originate from outside the
gastrointestinal tract. These are designated as extragastrointestinal stromal
tumors (EGISTs) [3].
Historically, these
lesions were classified as leiomyomas or leiomyosarcomas because they possessed smooth muscle features. With the
advent of immunohistochemical staining techniques GISTs now are recognized as a
distinct group of mesenchymal tumors. GISTs express c-kit protein also known as
CD117, and is considered a specific marker that differentiates GIST from other
mesenchymal tumors such as leiomyomas [4].
The most common
clinical manifestation for symptomatic GIST is pain in abdomen and GI bleeding
from mucosal ulceration [5]. Other presentations include mass in the
abdomen or intestinal obstruction. Endoscopy and colonoscopy clearly delineate
the site and macroscopic appearance. However, ultrasonography (USG) and
computerized tomographic (CT) scan are useful to determine the location of tumor
in the gastric or intestinal wall [6].
Tumors less than 2 cm in diameter with a mitotic rate of
&amp;lt;5/50 HPF (high power field) have been shown to have lower risk of recurrence
than larger tumors. All GIST tumors should be considered to have malignant
potential [7]. At present, surgery remains the mainstay of treatment for GIST. Recently,
imatinib mesylate has been introduced as an adjunct therapy for metastatic
disease, for non resectable tumor and for prevention of recurrence [5]. In this report, we describe the
socio-demographic characteristics, clinical presentations, anatomical location,
investigations, morphological variation, treatment and outcome of GIST
encountered over four years period at two tertiary care hospitals.
&amp;nbsp;
All
the patients diagnosed with GISTs from 2013 to 2016 at two tertiary care of
hospitals (BIRDEM General Hospital and Gastroliver Hospital) of Dhaka city were
included in the study.GIST
cases were analyzed for age, sex, clinical features, tumor location, size,
histological characteristics and CD117 marker. Types of surgery, post operative
event, outcome of imatinib therapy, disease recurrence, recurrence site and
survival rate were also analyzed. Mitotic figure defined as number of mitosis
per 50 HPF (high power field). Disease recurrence means local recurrence or
distant metastasis. GIST cases with inconclusive histological findings during
the study period were excluded. Long term follow up at intervals were done by
clinical examination, routine blood test and abdominal USG.
</description>

            </item>
            
    <copyright>2026 Ibrahim Medical College. All rights reserved.</copyright>
</channel>
</rss>
