Background: Adenosquamous carcinoma is a rare aggressive subtype of pancrea
tic adenocarcinoma, We describe the clinical, pathologic, and molecular cha
racteristics of 25 of these lesions, the largest series to date. Methods: T
wenty-five cases of adenosquamous carcinoma of the pancreas diagnosed betwe
en 1961 and 1994 were retrieved from the files of the Endocrine Registry of
the Armed Forces Institute of Pathology. Histologic features were reviewed
, histochemical, immunohistochemical, and molecular (k-ras) studies were pe
rformed, and patient follow-up was obtained. Results: The patients included
17 men and eight women, aged 28 to 82 years (mean, 65.4 y). The patients u
sually experienced weight loss (n = 17) or painless jaundice (n = II), whil
e also presenting with other abdominal symptoms. The tumors affected the he
ad most frequently (n = 17), followed by the tail (n = 9) or body (n = 4).
Five cases involved more than one anatomic region of the pancreas. Microsco
pically, all tumors demonstrated dual differentiation toward adenocarcinoma
and squamous cell carcinoma. All cases tested were immunoreactive with ker
atin (AE1:AE3 and CK1), whereas other keratin markers were variably express
ed: CK5/6 (88%), CK7 (68%), Cam5.2 (41%), and CK20(26%). CA-19-9 (84%) and
CEA (74%) were positive in the majority of the cases. K-ras oncogene mutati
ons were identified in seven of 13 cases. AH patients died from their disea
se an average of 5.8 months after diagnosis (range, 1 to 33 months). Conclu
sions: Adenosquamous carcinoma of the pancreas represents a distinct clinic
al and pathologic entity, demonstrating the expected immunoprofile and k-ra
s oncogene mutation of a ductal origin, with a worse prognosis than ductal
adenocarcinoma.