A man aged 42 years died from a hemorrhage resulting from stab wounds in his neck, chest and abdomen. The MN blood group and PGM1 phenotype of the victim's heart blood were inconsistent with those of the blood stains around the victim. The victim was transfused with 4000 ml of blood during the 9 hours before his death. Because PGM1 phenotypes obtained from blood stains at the scene of the crime and from the weapon corresponded with those from the victim's dental pulp, peripheral nerve and bone marrow, the victim's blood groups and isoenzymic phenotypes could be determined accurately.

ABO Blood-Group System↗

PubMedDate not supplied

The distribution of common phenotype of sperm diaphorase in the Japanese.

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Adult↗

PubMedDate not supplied

Significance of haemorrhages in central parts of the tongue found in the medicolegal autopsy.

The tongue was examined for the presence of haemorrhages in 264 medicolegal autopsy cases. The tongue was sectioned transversely and examined macroscopically and microscopically. Haemorrhages were found in marginal and/or central parts of the tongue in 104 cases. Among them, 28 cases showed haemorrhages in central parts of the tongue. Those haemorrhages in central parts of the tongue were seen only in cases of severe 'congestive death'. The possibility must therefore be considered of a severe 'asphyxial death', if haemorrhages are found in central parts of the tongue during autopsy.

Asphyxia↗

PubMedDate not supplied

[Serial changes of coronary arteries after percutaneous transluminal coronary angioplasty: histopathological and immunohistochemical study].

Intimal hyperplasia due to fibrocellular proliferation, mainly of smooth muscle cells, leads to restenosis after successful percutaneous transluminal coronary angioplasty (PTCA). The mechanism of intimal proliferation of smooth muscle cells was investigated by histological and immunohistochemical studies of necropsied coronary arteries from 13 patients who died between several hours and 1 year 8 months after PTCA. Immunohistochemical examinations clearly revealed smooth muscle cells already migrating from the media into the injured intima after 10 days. Thereafter, significant proliferation of smooth muscle cells was observed on the intimal side of the affected regions, predominantly around the circumference of the lumen at the PTCA site. Arteries from patients with restenosis who died more than 1 month after PTCA demonstrated proliferating cells with a polygonal shape and large bizarre nuclei. Arteries without restenosis showed smooth muscle cells with a spindle shape and rather elongated or oval nuclei. Although these cells were ordered along the luminal surface, the intercellular space still contained abundant ground substances. A case in which death occurred more than 1 year after PTCA showed these cells were analogous to medial smooth muscle cells. In addition, the extracellular matrix volume was extremely reduced, and composed chiefly of collagen as shown by positive Masson's trichrome stain. These histological findings demonstrated completion of repair and stabilization of the lesion caused by PTCA. Immunohistochemical investigation showed proliferating cells stained positive to vimentin but were negative to desmin, irrespective of the lesion age. This study provides pathological support for clinical reports suggesting that restenosis is predominant between 1 and 6 months and decreases beyond 1 year after PTCA.

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