Gastric plexiform angiomyxoid myofibroblastic tumour

Plexiform angiomyxoid myofibroblastic tumour (PAMT) of the stomach is a rare mesenchymal tumour predominantly involving the gastric antral region. There has been continued dispute about its nomenclature with other terminologies used for this tumour as plexiform angiomyxoid tumour, plexiform fibromyxoma. Pathologically, this tumour exhibit distinct morphological and immunophentypic features which aid in differentiating it from a wide range of differential diagnoses list. Here, in this paper, we present a case of PAMT with detailed discussion about its clinical profile, radiologic, and pathologic features including its histogenesis and differential diagnoses.