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Case Rep Gastroenterol. 2009; 3(1): 43–48.
Published online 2009 April 10. doi:  10.1159/000210437
PMCID: PMC2895175

Mucinous Cystadenocarcinoma of the Colon during Pregnancy

Abstract

A rare case of mucinous adenocarcinoma of the cecum in a pregnant woman is described. A 32-year-old Korean woman was diagnosed as having an abdominal tumor immediately after giving birth. Abdominal computed tomography demonstrated a smooth mass measuring 10 cm in diameter on the right side of the abdomen. Acute abdomen developed 3 days after birth. At emergency surgery, volvulus of a polypoid tumor was detected at the cecum apart from the normal appendix. We successfully performed a tumorectomy; however, histopathological examination demonstrated mucinous adenocarcinoma with a massive blood clot.

Key Words: Mucinous cystadenocarcinoma, Colon, Pregnancy

Introduction

Primary mucinous cystadenocarcinoma occurring in the colon is rare, moreover almost all such tumors occur at the appendix [1]. Mucinous cystadenocarcinoma of the intestinal tract is extremely rare. A polypoid lesion of mucinous cystadenocarcinoma has not previously been reported. Moreover, our case is extremely rare because volvulus of a polypoid tumor occurred in association with pregnancy.

Case Report

A 32-year-old Korean woman was admitted to the Shizuoka Municipal Shimizu Hospital in August 2007 to give birth. Three days after the birth, the patient suddenly developed acute epigastric pain. Board-like rigidity with rebound tenderness was noted in the epigastrium, and abdominal computed tomography (CT) demonstrated a 10 cm mass on the uterus (fig. (fig.1).1). Laboratory studies demonstrated a white blood cell count of 9,400/mm3, carcinoembryonic antigen level (CEA) of 40.7 ng/ml and carbohydrate antigen 19-9 (CA19-9) of 24,116 U/ml (table (table1).1). We thus diagnosed a volvulus of the tumor originating from the uterus. An emergency laparotomy was performed immediately, and a giant volvulus tumor originating from the cecum wall was identified (fig. (fig.2).2). The tumor was rotated about 540°. We resected the tumor and a normal appendix and uterus were confirmed. Macroscopically, the resected specimen showed an encapsulated, cystic tumor measuring 10 cm in diameter with a smooth surface that was connected to the cecum wall with a stalk (fig. (fig.3).3). The sections showed a blood clot. At the top of the tumor, atypical tubular structures with clear cytoplasm were seen only focally (fig. (fig.4).4). Ki-67 labeling was high. The features are compatible with mucinous cystadenocarcinoma. Immunohistochemical analysis showed CEA expression. Colonoscopy demonstrated negative findings up to the terminal ileum. The postoperative course was uneventful and the patient was followed by the outpatient department. Complete remission was achieved and no sign of recurrence has been observed in the 15 months after surgery.

Fig. 1
Abdominal CT demonstrated a low-density, encapsulated, thin-walled mass.
Fig. 2
a Giant volvulus tumor originating from the cecal wall. b After resection of the tumor. c Schematic representation of b. The tumor stalk was away from the appendix and uterus. a = Appendix, u = uterus, c = cecum, t = tumor stalk.
Fig. 3
Resected specimen showing the encapsulated cystic mass.
Fig. 4
Histological examination demonstrated that the tumor was a mucinous cystadenocarcinoma (H&E, ×100).
Table 1
Laboratory data

Discussion

Mucinous cystadenocarcinomas demonstrate high-grade cellular dysplasia and frequently invade the stroma beyond the muscularis mucosa [2]. Mucoceles of the colon are uncommon [1, 3]. Almost all such tumors occur at the appendix [2, 4, 5, 6]. To our knowledge, this is the first report of mucinous cystadenocarcinoma on the cecum wall during pregnancy.

Tumor marker levels during pregnancy are not significant [7]. Elevated CEA shows a high correlation with tumor recurrence and the presence of metastasis from colorectal cancer [8]. Chuang et al. [6] reported that the CEA level is elevated in mucinous cystadenocarcinoma. They suggested regular follow-up of the serum CEA level for the early detection of tumor recurrence. In our case, the serum CEA level was slightly elevated, but the serum CA19-9 level was extremely high. Postoperatively CEA and CA19-9 levels normalized.

The clinical symptomatology of mucocele of appendicitis patients is not specific. Abdominal pain is present in 64% of patients and a palpable ileocecal mass is found in 50% of cases [4]. Our patient demonstrated sudden onset of right lower quadrant abdominal pain three days after delivery. Pressure or release by the uterus might have led to volvulus of the tumor.

Sonography usually shows a cystic encapsulated lesion with liquid content [4, 5, 7]. CT scan shows a low-density, encapsulated, thin-walled mass that is not enhanced by contrast medium [2, 3, 4, 5, 6, 9]. Previously reported magnetic resonance imaging showed the same pattern as CT [7]. In our case, an encapsulated 10 cm diameter mass was located over the uterus on CT.

Mucinous peritoneal tumors tend to be associated with a poor prognosis, despite extensive treatment, including radical surgical excision and adjuvant intraperitoneal and systemic chemotherapy. The 10-year survival of patients with mucinous cystadenocarcinomas is 65% among patients treated with hemicolectomy and only 37% among patients who undergo appendectomy alone [5]. In our case, the malignant lesion was distant from the wall of the cecum and mesenterium. From this perspective, the patient selected adjuvant chemotherapy after sufficient explanation and informed consent.

In conclusion, we report a patient with volvulus of a cecal tumor after giving birth.

References

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Articles from Case Reports in Gastroenterology are provided here courtesy of Karger Publishers