A rare adenosquamous carcinoma of the colon occurred in a 41-year-old patient. Its presentation with hypercalcemia, in the absence of osseous metastases, has not been described previously. The hypercal-cemia in this case was due to the elaboration of a parathyroid hormone-like substance by the tumor. The general characteristics of primary adenosquamous and squamous cell carcinomas of the colon are presented. These tumors present with advanced disease, in younger patients, and follow a highly aggressive course, as compared with adenocarcinomas of the colon. The cause of the malignancies, in the light of current theories regarding their genesis, is discussed. Cancer60:1111-1116, 1987. RIMARY ADENOSQUAMOUS and squamous carci-P noma of the colon are extremely rare entities. Approximately 60 cases have been reported. The incidence in a number of series has been estimated to be 0.25 to 0.5 cases per 1000 colon malignancies.'-* The coincident finding of hypercalcemia in a colon malignancy has been reported in only three previous ~ases~,~-only one was a case of adenosquamous c a r ~ i n o m a. ~ In the case of adenosquamous carcinoma, the patient had diffuse bony metastases, and a normal parathyroid hormone level. In the other two cases a parathyroid hormone-like substance was identified in the tumor cells of one patient , thus explaining the cause of the hypercalcemia, whereas the cause of the hypercalcemia in the other patient was not a~certained.~ To these we add another rare case, one in which a parathyroid hormone-like substance was identified in an adenosquamous carcinoma of the colon. Case Report A 4 1-year-old woman was admitted to the surgical oncology service at SUNY-Stony Brook's University Hospital in Jan-uary 1986. She complained of weakness, cachexia, nausea, and vomiting. Her complaints began in November 1985, when she was seen by her private physician for abdominal pain. A uri-nary tract infection was diagnosed and treated with antibiotics. She continued to feel poorly, however, and was subsequently admitted to another hospital, where she received intravenous antibiotics. She was then readmitted in December 1985, at which time hepatomegaly and multiple liver nodules were noted. The biopsy specimen of her liver disclosed metastatic adenocarcinoma, and she was referred to University Hospital. Her history was significant for total abdominal hysterectomy and bilateral salpingo-oophorectomy for leiomyomata, and peptic ulcer disease. On physical examination she was noted to be extremely cachectic and in moderate distress. Her abdomen was soft with mild diffuse tenderness. The liver was nodular and hard, and palpated 4 inches below the costal margin. Findings of rectal and pelvic examinations were negative. The stool guaiac was negative. Admission laboratory studies showed the following values: hemoglobin, I0 g/dl; he-matocrit, 33.2%; calcium, 18.4 mg/dl; phosphate, 4.9 U/dl; albumin, 3.9 g/dl; lactate dehydrogenase (LDH), 2267 U/l; aspartate aminotransferase (AST), 66 U/I; alanine aminotrans-ferase (ALT), 41 U...