An Unexpected Pregnancy Test Result Leading to the Diagnosis of Advanced Gastric Cancer.

The presence of beta human chorionic gonadotropin in the absence of pregnancy warrants further workup as elevated levels may be seen in trophoblastic disease or germ cell tumors and rarely in solid tumors such as gastric cancers. The signs and symptoms of gastric cancer are vague and as such, the diagnosis is often delayed. Overexpression of the beta-subunit of human chorionic gonadotrophin may be seen in close to 50% of gastric cancers. The implication of this finding is unclear; however, beta human chorionic gonadotropin reactivity may play a role in tumorigenesis and often correlates with an advanced stage at presentation. Herein, we present a case report of a patient with an incidental finding of a positive urinary human chorionic gonadotropin test which led to the diagnosis of advanced gastric cancer.

Introduction

Gastric cancer is one of the leading causes of cancer-related deaths in the world and a significant contributor of morbidity. The initial symptoms are often vague which delays diagnosis. In fact, the symptoms of unexplained weight loss, epigastric bloating, early satiety and persistent vomiting usually represent locally advanced or widespread metastatic disease [1].

The use of tumor markers such as carbohydrate antigen 19–9 (CA 19–9), carcinoembryonic antigen (CEA), cancer antigen 125 (CA-125) and cancer antigen 72–4 (CA 72–4) have been suggested for pre and post-operative monitoring of the evaluation of resection and/or recurrence [2]. The combination of these markers has been shown to increase diagnostic sensitivity. There have also been emerging studies which show that close to 50% of gastric cancers may express the beta-subunit of human chorionic gonadotropin (βHCG), a tumor marker that may correlate with a high tumor burden. In the absence of pregnancy and trophoblastic tumors, elevated βHCG is ominous for malignancies such as osteosarcoma, testicular seminoma pancreatic cancer and gastric carcinoma [3]. Here we present the case of a non-pregnant woman with gastric carcinoma who was diagnosed after incidental finding of a positive βHCG.

Case Presentation

A 47-year-old Afro-Caribbean female with a past medical history of uterine fibroids presented with vague symptoms of intermittent abdominal pain, nausea and vomiting for two weeks. Her last menstrual period was one week prior to presentation and the patient reported being celibate for the past 4 years. She denied weight loss, early satiety or change in bowel habit. The rest of the history was unremarkable. The initial examination revealed normal vital signs and generalized abdominal tenderness without rebound or guarding. Lab investigations were significant for hemoglobin 8 (12–15g/dL), MCV 80.4 (80–96 fL/red cell), Iron 14 (40–155ug/dl), TIBC 265 (240– 450 ug/dl) and Ferritin 9.9 (12–150ng/dl), alkaline phosphatase 476 (40–100 U/L) and a positive urine βHCG. The renal indices and other hepatic function tests were within normal limits. A transabdominal ultrasound showed an intramural uterine density and no evidence of an intrauterine pregnancy. Serum βhCG was 75.0 (0–5mIU/ml).

The patient was referred to the gynecology service who determined that pregnancy was unlikely and ordered a CT abdomen-pelvis to evaluate the density in the uterus. This study revealed multiple scattered retroperitoneal, celiac axis, gastrohepatic ligament and pelvic lymph nodes measuring up to 1.4cm in short axis suspicious for metastatic disease or lymphoma. It also showed ascites, 2 small uterine fibroids, ill-defined heterogenous density along uterine fundus and a 1.9cm soft tissue nodule adjacent to the spleen. The imaged osseous structures appeared sclerotic.

Histological examination of a biopsied left para-aortic lymph node showed poorly differentiated metastatic adenocarcinoma with signet cell features suggestive of a gastric primary [Figure 1]. Subsequent esophagogastroduodenoscopy was remarkable for irregular gastric mucosa, biopsy of which revealed poorly differentiated adenocarcinoma [Figure 2], HER-2 receptors were negative and there was no evidence of Helicobacter Pylori infection.

Figure 1.

H&E stain of left para-aortic lymph node. High power magnification showing poorly differentiated metastatic adenocarcinoma with < 50% signet ring features (red arrows)

Figure 2.

H&E stain of gastric mucosa. Low power magnification showing solid sheets of tumor cells (poorly differentiated) with minimal gland formation (blue arrow)

The patient was initiated on Cisplatin and 5-Fluorouracil and after 2 cycles had transient improvement of her (3HCG levels to 45 (0–5mIU/ml). She subsequently developed recurrent exudative pleural effusions with cytology that was negative for malignancy. Although cyto logy was negative, the effusions were thought to be due to gastric cancer. Profound thrombocytopenia and pulmonary hemorrhage then developed, and she had cardiac arrest. The patient passed away within 3 months of initial diagnosis.

Discussion

Gastric cancer is the fifth most common cancer worldwide with an estimated incidence of 952,000 cases in 2012 [4]. Approximately 70% of these cases occur in developing countries with a strong preponderance in East Asia. This cancer still carries a high mortality and is the 3rd most lethal cancer with mortality rates of 723,000 [4]. Patients with gastric cancer are often asymptomatic in the early stages when resection of the primary lesion could effect cure. Instead, most patients present with advanced or widely metastatic disease which may manifest with symptoms of unintentional weight loss, early satiety, abdominal bloating or distention and gastrointestinal bleed from an ulcerated lesion [1]. Several risk factors, including Helicobacter pylori infection, family history of gastric cancer, history of chronic atrophic gastritis, smoking, heavy alcohol consumption, obesity and low socioeconomic status, may contribute to the development of gastric cancer [1,5]. Of these, Helicobacter pylori infection has been found to be most closely related to the occurrence of gastric cancer. The process appears to be multifactorial and involves host and environmental factors. There has however been a decline in the prevalence of Helicobacter Pylori in some developed countries due to improved hygiene and food preparation a s well as increased use of antibiotics [5].

There are currently no specific tumor markers that have adequate sensitivity or specificity for diagnosis or follow-up of gastric cancer. However, serum levels of CEA, CA 125, CA 1 9–9, CA 72–4 and even less commonly βhCG may be elevated in patients with gastric cancer and are associated with a poorer prognosis [2]. However, the use of these of markers have not been standardized in clinical practice. Human chorionic gonadotropin is normally produced by the syncytiotrophoblast cells of the placenta and is used to detect and monitor pregnancy. The beta-subunit of hCG is a sensitive and specific marker for trophoblastic tumors of placental and germ cell origin [6]. It can also be falsely elevated in hypogonadal states, exogenous administration and marijuana use. Outside of these contexts elevated levels of βhCG are usually associated with malignancies such as breast cancer, leiomyosarcoma, pancreatic cancer, lymphoma and leukemia [6]. It may also be elevated in other malignancies, such as gastric cancer, with an undefined sensitivity or specificity [2]. The role of βhCG in the progression of gastric cancer remains unclear but its presence is usually consistent with a more poorly differentiated tumor and associated worse prognosis [3,6].

In evaluating patients with elevated βhCG levels, work-up for malignancy must be performed once pregnancy is ruled out. The work-up should not be limited to the tumors that are conventionally associated with elevated βhCG but should also be expande d to include a broad base of organs. This approach is strongly warranted as the presence of this hormone may signify the presence of an insidious but aggressive malignancy and has significant prognostic implications.