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Large Jejunal Gastrointestinal

Stromal Tumor Presenting as


Intestinal Obstruction
A CASE REPORT
Dr. Nayef Al Abedallat Dr. Omar Suleiman
Head of Surgery Department Resident General Surgery
Zarqa New Governmental Hospital
Introduction Case Report
GISTs are the MC mesenchymal neoplasms of the GI tract . A 65-year-old male with medical history of hypertension and diabetes
Although they account for less than 1% of all GI tumors. mellitus, previously surgically free.
The incidence of GIST tumors is 1–2/10^5 population Presented to the ED with diffuse abdominal pain and distention.
GISTs arise usually from the muscularis mucosa or propria layers  Nausea, vomiting and constipation for 5 days.
GIST arises most commonly from: On PE:
 The stomach (60–70%), followed by small bowel (20–25%).  Vital signs were normal and stable, patient was afebrile.
 Of which jejunal GISTs are the rarest subtype.  Abdominal distention, generalized tenderness and a palpable epigastric
They usually present with non-specific symptoms: mass.
 Abdominal pain, epigastric mass and GI bleeding .  Absent bowel sounds and an empty rectum.
Tumors larger than 4 cm may present as abdominal emergencies:  CBC, Urine analysis, Serum Chemistry were requested
 Including GI hemorrhage, intestinal obstruction, or perforation.  all normal except for low Hb.
 An abdominal X-ray revealed small bowel obstruction pattern.
 Ultrasonography examination revealed mass lesion with solid and cystic
areas in the mesentery attached to small intestine suggestive of mesenteric
mass (? mesenteric cyst).
 A CT scan of the abdomen and pelvis was requested
 Identified a large 10*15 CM mass obstructing the small bowel with solid
and cystic components, with no evidence of distant metastasis.
 The patient previously complained of vague epigastric abdominal pain for 3
years, and extensive investigations including blood tests, OGD, colonoscopy
and even a CT scan were requested, and all investigations were normal on
multiple occasions.
 Emergency laparotomy was performed with excision of the mass along with
small bowel resection and primary end to end anastomosis
 On histopathological reports, the lesion was composed of areas of spindle
and epithelioid cells, and immunohistochemical analysis showed positive
staining with CD117 consistent with GIST
 The postoperative period was uneventful, and the patient was discharged
after 7 days and commenced on imatinib for 3 years.

Conclusion
This case was reported due to the rare incidence of jejunal GISTs
To highlight the challenges in diagnosing jejunal GISTs .
To stress the fact that although obstruction from GIST tumors of
the small bowel is a rare occurrence, but still it might happen.
To raise awareness of GISTs and to raise the level of suspicion
required for the diagnosis of such a rare entity.
Better understanding of the cell of origin and
immunohistochemical markers has made targeted therapy
possible in GIST.
 GISTs treatment has been revolutionized with the introduction
of imatinib.

The 47th Conference of JSS & the 7th Conference of


Surgical Specialty / MOH

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