Keywords

1 Introduction

There are 2 different histological types of esophageal carcinoma (squamous cell- and adenocarcinoma) with different characteristics such as location (primarily upper esophagus for SCC and lower for adenocarcinoma) and risk factors (alcohol and smoking for SCC vs. gastroesophageal reflux and Barretts esophagus for adenocarcinoma) [1]. As adenocarcinoma is the commonest, discussion is referring mainly to this particular histological type [2].

Esophageal adenocarcinoma presents with solid food dysphagia and weight loss and is diagnosed with upper gastrointestinal endoscopy and biopsies.

Both prognosis, which unfortunately remains poor [3] and therapeutic algorithm (neoadjuvant therapy before surgery, endoscopic resection vs. surgery) depends on staging.

With regards to gastric cancer, the majority of patients has limited symptoms (weight loss and abdominal pain) or is completely asymptomatic and present with advanced, metastatic and thus incurable disease.

The diagnosis is made with upper gastrointestinal endoscopy and biopsies where at least 7 biopsies are thought to be needed to increase diagnostic accuracy [4]. In a particular type of diffuse-gastric cancer (linitis plastica) apart from sufficient number, a specific endoscopic biopsy technique is advocated to ensure adequate tissue sample (strip and bite biopsy technique). In these cases, Barium study is a useful diagnostic tool with the characteristic ″leather flask" appearance of the stomach due to poor distensibility.

MALT is one of the most common histologic types of gastric lymphoma which is diagnosed with endoscopy and biopsies.

Staging investigations include CT chest, abdomen and pelvis (distant disease-M stage) and EUS (depth of invasion-perigastric lymph nodes-T and N stage).

GISTs are stromal or mesenchymal tumors that can present as subepithelial masses anywhere in the gastrointestinal tract (more often in the stomach rather than the esophagus where leiomyomas are the commonest) including rarely mesentery, omentum and peritoneum. The majority are sporadic with a mutation in the KIT or much less frequently in the PDGFRA gene [5].

They affect predominantly middle-aged or older individuals and typically present with no or nonspecific symptoms (bloating, early satiety) unless they are complicated by ulceration, bleeding or intestinal obstruction.