On reading the literature describing the histopathology of visceral leishmaniasis in man and animals, one is struck not only by the heavy involvement of spleen, liver, and bone marrow (Christophers, 1904; Shortt, 1923-24; Meleney, 1925) but by the diversity of the other organs in which leishmania may be found in focal o r extensive lesions. A representative sample would be small intestine (Perry, 1922), facial mucocutaneous a r e a s (Kirk, 1942), vaginal mucosa (Symmers, 1960), larynx (Sati, 1962, testis, prostate, meninges and lungs. A late reference to this varied distribution is Manson-Bahr's statement (1959) that in man "leishmania can b e found in any organ, the blood or the skin." With such diversity, it would be expected that the variability from patient to patient o r animal to animal would be considerable.In contrast to this a r e the findings using intracardially (IC) infected golden hamsters, where organs other than the spleen, liver, and bone marrow a r e less frequently involved, even though infected lymphoid cells may b e observed in blood smears late in the infections.Laveran (1917) made an important pertinent observation, stating that the extent to which organs other than the spleen, liver, and bone marrow a r e involved in kala azar is determined by the intensity and duration of the infection.The intracardial route of infection leads to earlier death in the golden hamster through visceral leishmaniasis (Stauber, 1955), a s contrasted with natural o r experimentally induced infections in man and some other animals. For example, one Chinese hamster was not necropsied until 455 days after inoculation (Meleney, 1925), whereas deaths as early as 28 days have been seen in the golden hamster when infected intracardially. Time may be an important variable in the distribution of lesions under such conditions.The parasites themselves may be another such variable. Even for those designated Leishmmia donouaizi, various isolates show different properties upon close examination. Morphological and cultural traits have not been very helpful in these distinctions. Adler (1963), however, has recently made prog r e s s using serological techniques, and others have found iiz uivo strain differences (Goodwin, 1945;Stauber, 1966) which a r e probably more pertinent to the present discussion. Still, there is no evidence yet that these strains result in host organ localizations of a specific nature. From the wide variety of clinical manifestations in the cases of kala azar reported for man, and especially from East Africa where an especially wide range of these variations occurs involvingboth skin and viscera, the parasites 635