Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT06242457 |
Other study ID # |
HU |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
July 15, 2023 |
Est. completion date |
December 30, 2023 |
Study information
Verified date |
February 2024 |
Source |
Haramaya Unversity |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Our study is a case report of one of the rarest risk factor, Peutz-Jeghers syndrome, of small
bowel malignancy detected in a patient with poorly differentiated adenocarcinoma of small
bowel(jejunum)
Description:
Case presentation: A 25-year-old male patient presented to the emergency department with
generalized peritonitis caused by a perforated jejunal mass. The patient underwent an
emergency exploratory laparotomy. There was 800 ml of thin pus in the peritoneal cavity and 5
cm by 6 cm perforated mass over the jejunum, 30cm from the ligament of the treitz, which
extends to the mesentery. Palpable jejunal mesenteric lymphadenopathies were found. There
were palpable intraluminal polyps with an inverted serosal surface for some of them, which
were identified as 10cm proximal and 20cm distal to the mass. The pus was sucked out, and the
mass was resected with its mesenteric lymph nodes and segments containing polyps, a total of
40cm of jejunum. Subsequently, end-to-end hand-sewn anastomosis was performed, and the
abdomen was closed. The histopathology report showed poorly differentiated adenocarcinoma,
stage IIIC (PT3, PN2), and Peutz-Jeghers polyps, suggesting Peutz-Jeghers syndrome.
Lympho-vascular invasion was also noted. The tumor has affected seven of the 12 lymph nodes
that have been identified. After 6weeks of uneventful follow-up at the surgical referral
clinic, the patient was referred to the oncology department for adjuvant chemotherapy.