وثيقة
Primary gastric Yolk Sac tumour.
المعرف
doi: 10.18295/squmj.2018.18.03.020
المساهمون
Al-Moundhri, Mansour., مؤلف
Al-Shaibiyah, Maha., مؤلف
Al-Haddabi, Ibrahim., مؤلف
Mittal, Alok., مؤلف
عناوين أخرى
ورم كيس محي أولي في المعدة
الناشر
College of Medicine, Sultan Qaboos University.
ميلادي
2018-02
اللغة
الأنجليزية
الموضوع
الملخص الإنجليزي
Primary gastric yolk tumours are extremely rare. We report a 52-year-old male who presented to the
Sultan Qaboos University Hospital, Muscat, Oman, in 2017 after having undergone a gastrectomy abroad due to
a suspected poorly-differentiated adenocarcinoma. The patient subsequently returned to Oman to receive chemo therapy. However, while undergoing chemotherapy, an abdominal computed tomography scan revealed a lobulated
mesenteric mass. Microscopic examination of the resected lesion confirmed a diagnosis of a yolk sac tumour. The
mass was diffusely positive for α-fetoprotein (AFP) and a gastric carcinoma stain was negative. Gastrectomy slides
from the patient's previous surgery were examined retrospectively. The morphology was typical for a yolk sac
tumour and was negative for epithelial markers. An AFP stain showed diffuse immunoreactivity. Thus, the patient was
deemed to have had a primary gastric yolk sac tumour which had later metastasised to the mesocolon. Germ cell
tumour protocols were initiated and the patient responded well to treatment.
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