- Open Access
Clinicopathologic features and outcomes following surgery for pancreatic adenosquamous carcinoma
© Hsu et al; licensee BioMed Central Ltd. 2008
- Received: 26 May 2008
- Accepted: 03 September 2008
- Published: 03 September 2008
Pancreatic adenosquamous carcinoma (ASC) is a rare pancreatic malignancy subtype. We investigated the clinicopathological features and outcome of pancreatic ASC patients after surgery.
The medical records of 12 patients with pancreatic ASC undergoing surgical treatment (1993 to 2006) were retrospectively reviewed. Survival data of patients with stage IIB pancreatic adenocarcinoma and ASC undergoing surgical resection were compared.
Symptoms included abdominal pain (91.7%), body weight loss (83.3%), anorexia (41.7%) and jaundice (25.0%). Tumors were located at pancreatic head in 5 (41.7%) patients, tail in 5 (41.7%), and body in 4 (33.3%). Median tumor size was 6.3 cm. Surgical resection was performed on 7 patients, bypass surgery on 3, and exploratory laparotomy with biopsy on 2. No surgical mortality was identified. Seven (58.3%) and 11 (91.7%) patients died within 6 and 12 months of operation, respectively. Median survival of 12 patients was 4.41 months. Seven patients receiving surgical resection had median survival of 6.51 months. Patients with stage IIB pancreatic ASC had shorter median survival compared to those with adenocarcinoma.
Aggressive surgical management does not appear effective in treating pancreatic ASC patients. Strategies involving non-surgical treatment such as chemotherapy, radiotherapy or target agents should be tested.
- Pancreatic Head
- Body Weight Loss
- Adenosquamous Carcinoma
- Cumulative Survival Rate
- Chang Gung Memorial Hospital
Adenocarcinoma accounts for the majority of pancreatic malignancies. Adenosquamous carcinoma (ASC) of the pancreas is an unusual variant of pancreatic neoplasm [1–4], and is characteristic by histological patterns of both ductal adenocarcinoma and squamous carcinoma within the same tumor. The prognosis of this rare tumor appears to be even less favorable than the common invasive ductal tumor with few patients surviving more than 1 year after surgical resection . Most of studies on this disease have been small series or single case reports, and few studies have investigated the clinicopathologic features and outcome of patients with pancreatic ASC following surgical treatment [1, 2, 5, 6]. Therefore, medical records of 12 patients with pancreatic ASC treated surgically at Chang Gung Memorial Hospital (CGMH), Taoyuan in the past 14 years were retrospectively reviewed.
A total of 637 patients with pancreatic malignancies underwent surgical treatment at CGMH between January 1993 and December 2006. Adenocarcinoma was diagnosed in 530 patients and ASC in 12. Institutional Review Board approval was obtained and medical records of 12 patients with pancreatic ASC were retrospectively reviewed. Preoperative imaging studies employed abdominal ultrasonography, abdominal computed tomography (CT)/magnetic resonance imaging (MRI), and endoscopic retrograde cholangiopancreatography (ERCP). Serum tumor markers such as carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA 19-9) were measured preoperatively. One patient had a preoperative fine needle tumor biopsy. Intraoperative radiotherapy and postoperative chemotherapy were performed in 2 patients and 7 patients, respectively. Tumor stage and TMN stage were defined according to the sixth edition of American Joint Committee on Cancer for pancreatic carcinoma  based on the histopathologic examination of surgical specimens and clinical findings such as imaging studies and intraoperative records. To further elucidate the outcome following surgical resection for pancreatic ASC from more common pancreatic adenocarcinoma, patients with stage IIB pancreatic adenocarcinoma undergoing surgical resection were also extracted from our databank (at the same studying period as pancreatic ASC). Survival data of patients with stage IIB pancreatic adenocarcinoma and ASC undergoing surgical resection were compared. Survival rate was calculated and graphs plotted using Kaplan-Meier method. Differences in survival curves between the groups were compared by the log-rank test. A p-value less than 0.05 were defined as statistically significant. All statistical analyses were performed with SPSS for Windows, version 11.5 (Statistical Package for the Social Science, SPSS, Inc., Chicago, Illinois).
Demographics of 12 patients with pancreatic adenosquamous carcinoma.
CA 19-9 (U/mL)
Abd pain, BWL, jaundice
BWL, jaundice, anorexia
Abd pain, BWL, diarrhea
HTN, heart disease
Abd pain, BWL
Abd pain, anorexia
Abd pain, BWL, anorexia, abd mass
Abd pain, BWL, jaundice
Abd pain, dizziness, malaise
HTN, DM, Peptic ulcer
Abd pain, BWL
Abd pain, BWL
Abd pain, BWL, anorexia
Abd pain, BWL, anorexia, malaise
Details of tumor characteristics, management, and prognosis of 12 patients with pancreatic adenosquamous carcinoma.
Body and tail
subtotal P, total G, S
distal P, S
distal P, total G, S
Body and Tail
subtotal P, S
The first report of ASC is credited to Herxheimer in 1907 . This admixed tumor has been seen more commonly in other organ systems where adenocarcinomas are generally found, such as the stomach , intestine  and uterus . It has also been identified in the esophagus , anus  and vagina  where squamous cell carcinomas predominate. In the present studies, the incidence of pancreatic ASC was 1.9% (12/637), within the range of 0.9 to 3.8% reported in the literatures [2–4]. The histogenesis of pancreatic ASC remains unclear. There are numerous possibilities that account for the presence of a squamous element where adenocarcinoma is expected. Four theories regarding the histogenesis of adenosquamous carcinoma may be summarized as follows: adenocarcinoma transforming into squamous cell carcinoma; bipotential undifferentiated cell origin; collision tumor; and squamous metaplasia origin .
Madura et al.  reported that most patients with pancreatic ASC are males in their 60s and frequently located at the head of the pancreas. Different from their findings, more females were identified in our patients, and the patient median age was 71 years. Moreover, our results show that the tumor location was evenly distributed at the pancreatic head, body, or tail. Symptoms of our patients with pancreatic ASC were abdominal pain (92%), body weight loss (83%), anorexia (42%) and jaundice (25%) similar to those of pancreatic adenocarcinoma .
Accurate preoperative diagnosis of pancreatic ASC is made with great difficulty since there are no investigations of its defining characteristics in imaging studies that would differentiate it from the more common pancreatic exocrine neoplasm . Nevertheless, studies have indicated that cytological examination of pure pancreatic juice obtained by endoscopic retrograde pancreatic juice aspiration is a useful modality for the preoperative diagnosis . Rahemtullah et al.  also reported that cytological features derived from fine-aspiration biopsy are diagnostic of pancreatic ASC. Furthermore, imaging studies by Nabae et al.  showed that the presence of central necrosis in a huge infiltrative pancreatic tumor is suggestive of the diagnosis of ASC. Moreover, a tumor might selectively take up gallium 67 and be visualized by nuclear scanning which is useful in detecting this rare pancreatic tumor . In the present studies, no patient had central necrosis at the pancreatic tumor on abdominal imaging studies indicating a diagnosis of pancreatic ASC. Besides, the preoperative fine needle biopsy of the tumor was performed in 1 patient, which revealed adenocarcinoma.
As shown in table 2, 11 patients with pancreatic ASC (92%) died within 12 months despite aggressive surgical management along with intraoperative irradiation or postoperative chemotherapy. The median cumulative survival of 12 patients was 4.92 months (Figure 2). Furthermore, median survival of 7 patients undergoing surgical resection was 6.51 months. These results were similar to that obtained by Madura et al. , who reported that 72 patients survived with an average age of 5.7 months, regardless of whether or not surgical resection was performed. To our surprise, 1 patient in our series who had no lymph node involvement without undergoing surgical resection and received intraoperative irradiation had a survival of 22.42 months. No lymph node metastasis and the potential benefit of intraoperative radiation therapy might explain his long survival.
Once pancreatic ASC is identified either preoperatively or intraoperatively, the choice of treatment becomes a complex decision as survival is typically dismal . In this regard, although PD has been shown to be performed with a very low mortality rate (<4%) in specialized high-volume centers, the incidence of postoperative morbidity can be as high as 30% to 40% [19, 20]. Furthermore, a significant high mortality rate (25%) has been reported in the patient subgroup with significant preoperative comorbidities . Thus, anesthesia risks and complications following major surgery in pancreatic ASC patients along with severe medical diseases should be considered before operation. Moreover, we observed that median survival of patients (stage IIB) with pancreatic ASC undergoing surgical resection was 6.51 months, significantly shorter (p = 0.018) than patients with stage IIB pancreatic adenocarcinoma receiving resection (median survival, 9.76 months; Figure 3), suggesting more aggressive biology of pancreatic ASC than adenocarcinoma. Moreover, nodal metastases were identified in 92% (11/12) of our patients, which might reflect the disease entity tending to have lymph node involvement and at least partly explained the poor prognosis of this virulent tumor.
It should be noted that this study was based on a retrospective review of patients undergoing surgery. Pancreatic malignancy patients who were not diagnosed as pancreatic ASC without tissue proof treated non-surgically were not enrolled in this study. Whether surgical resection or non-surgical management such as chemotherapy, radiotherapy, chemo-radiotherapy or target therapy would provide survival benefits to patients with pancreatic ASC remains unknown. More studies are necessary to confirm this.
Pancreatic ASC is a rare pancreatic neoplasm subtype. Abdominal pain and body weight loss are the two predominant symptoms. Distribution of ASC is even in the pancreas, and the tumor size is big at the time of diagnosis. Pancreatic ASC tends to have nodal metastases and has a dismal outcome despite surgical resection. In this limited case study, aggressive surgical management does not appear effective in treating pancreatic ASC patients. Strategies involving non-surgical treatment such as chemotherapy, radiotherapy or target agents should be tested.
We thank Yi-Hua Liu for assistance with data collection and Shu-Fang Huang for superb help with data analysis and preparing the tables and figures.
The written consent was obtained from the patients' Family for publication of this study and IRB approval was obtained for collecting the data.
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