The current study attempts to clarify the possible immune response that occurs in medullary carcinoma with lymphocytic infiltration of the stomach by an immunohistochemical analysis of the subpopulations of tumor-infiltrating lymphocytes. This carcinoma was histologically characterized by the sparse population of small nests consisting of poorly differentiated carcinoma cells, widely separated by intervening nondesmoplastic stroma infiltrated uniformly with abundant lymphocytes frequently accompanied by lymph follicles. An immunohistochemical analysis revealed that T-cells were evenly distributed throughout the tumor with intimate contact with individual carcinoma cells, except the lymph follicles consisted mainly of B-cells. Because of the similarities of morphologic features and subpopulations of tumor-infiltrating lymphocytes of this carcinoma to the normal lymphoid tissue, an organized immune response combined with cell-mediated and humoral immunities against the invading carcinoma cells seemed to occur in this type of gastric carcinoma, resulting in a excellent prognosis compared with that in ordinary gastric carcinoma. Cancer 66:945-952.1990. N CARCINOMAS of the stomach and other organs, many I investigations have been conducted to correlate the mode of lymphocytic infiltration in the tumor with the postoperative survival of patients. '-' As for breast carci-noma, it is well known that medullary carcinoma with lymphoid infiltration has a less ominous prognosis. With its close histologic resemblance to and its similar favorable prognosis compared with the medullary carcinoma of breast, a unique type of gastric carcinoma with significant stromal lymphocytic infiltration has been noticed. Several

A series of poly(6-azulenylethynyl)benzenes substituted with n-hexyloxycarbonyl chains at 1,3-positions in azulene rings, i.e., hexakis-, 1,2,4,5-tetrakis-, 1,3,5-tris-, and 1,4-bis(6-azulenylethynyl)benzene derivatives 1, 2, 3, and 4b, have been prepared by a simple one-pot reaction involving repeated Pd-catalyzed alkynylation of halogenated arenes with substituted 6-ethynylazulene and/or ethynylated arenes with substituted 6-bromoazulene under Sonogashira-Hagihara conditions. The redox behavior of these novel poly(6-azulenylethynyl)benzene derivatives was examined by cyclic voltammetry (CV), which revealed the presumed multielectron redox properties. Compound 4b exhibited a one-step, two-electron reduction wave upon CV, which revealed the formation of the dianion stabilized by two 6-azulenylethynyl substituents under electrochemical reduction conditions. Four 6-azulenylethynyl substituents on a benzene ring in a 1,2,4,5 relationship increased the electron-accepting properties because of the formation of a stabilized closed-shell dianionic structure, whereas 3 was reduced at more negative reduction potentials. In contrast to the multistep redox behavior of 2, compound 1 was reduced in one step at -1.28 V upon CV. Compound 1 showed a wide temperature range of columnar mesophases (Col(ho) and Col(ro)) from 77.3 degrees C to the decomposition temperature at ca. 270 degrees C. Compounds 2, 3, and 4b exhibited columnar mesomorphism (Col(ro)) with crystalline polymorphs for 2, unusual triple-melting behavior for 3, and both double-melting behavior and columnar mesomorphism (Col(ho)) for 4b. Therefore, the investigated systems exemplify a new principle for multielectron redox behavior with liquid crystalline properties.