½Ã¹ÝÀÌ À̵¿µÇÁö ¾Ê´Â ÀÌÀ¯ (½Ã¹ÝÀÇ °íÁ¤, ¾çÃø¼º ½Ã¹Ý, °íÁ¤ ½Ã¹Ý)
½Ã¹ÝÀÇ º¯À§°¡ ÀϾÁö ¾Ê°Å³ª ½Ã¹ÝÀÇ À̵¿ÀÌ ¾ø´Â °ÍÀº ÀÌÁ¦±îÁö´Â ÀÚ°¡¿ëÇ÷·Î ÀÎÇÑ Çì¸ð±Û·ÎºóÀÇ Á¶±â È®»ê ¶§¹®À̶ó°í ¾Ë·ÁÁ® ¿ÔÀ¸³ª
»ç½ÇÀº Èú°Å¸¸ÀÇ À̷дë·Î À¯Ã¼Á¤¿ªÇÐ(êüô÷ð¡æ³ùÊ) ¾Ð·Â°ú °ü·ÃµÈ °ÍÀ¸·Î Ç÷°ü º®À» Åë°úÇÏ´Â Ç÷¾×³»ÀÇ ¾×ü ¼Õ½Ç·Î ÀÎÇÑ ³óÃà(hemoconcentration) ¶§¹®ÀÌ´Ù.
The reason for non-displacement and non-shifting of lividity is not the early diffusion of haemoglobin, as supposed formerly, but the haemoconcentration by loss of fluid which penetrates the wall of those vessels related to the hydrostatic pressure, as shown by Hilgermann.
The Estimation of the Time Since Death in the Early Postmortem Period, 1995, Edward Arnold; C Henssge, B Knight, T Krompecher; pp241
ÀϺ»ÀÇ Noriko ±³¼ö´Â ½Ã¹ÝÀÇ °íÁ¤ ¸ÅÄ¿´ÏÁòÀ» ¾Ë±â À§ÇØ ¸é¿ªÁ¶Á÷ÇÐÀû ¿¬±¸¸¦ Çß´Ù. »ç¸Á ÈÄ 7.5 ½Ã°£ºÎÅÍ 2ÁÖ±îÁöÀÇ 68±¸ »çü¿¡¼ ÇǺΠÁ¶Á÷À» °Ë»çÇÏ¿´´Ù. Ç÷»ö¼Ò°¡ ħÅõµÈ ÇǺΠÁ¶Á÷ÀÇ ¿©·¯ ºÎÀ§º° (¿¹¸¦ µé¸é Ç÷°ü³» ÀûÇ÷±¸, Ç÷°üº®, Ç÷°üÁÖÀ§Á¶Á÷, ÁøÇÇ°áÇÕÁ¶Á÷) °Ë»ç¸¦ ½ÃÇàÇß´Ù. Áö¾ÐÈçÀÌ °üÂûµÇ´Â °÷¿¡¼´Â 49%°¡ °íÁ¤½Ã¹ÝÀÌ ÀÖ´Â °÷¿¡¼ 41%¿¡¼¸¸ Ç÷»ö¼ÒÀÇ ÇǺÎÁ¶Á÷ È®»êÀÌ °üÂûµÇ¾ú´Ù. ÀÌ·¯ÇÑ ¼Ò°ßÀº ½Ã¹ÝÀÇ °íÁ¤ÀÌ Ç÷»ö¼ÒÀÇ È®»ê ¶§¹®ÀÌ ¾Æ´Ï¶ó Ç÷¾×ÀÇ ³óÃà ¶§¹®À̶ó´Â °¡¼³À» µÞ¹ÞħÇØÁØ´Ù.
An immunohistochemical investigation of postmortem lividity was performed to illuminate localization of hemoglobin (Hb) and the mechanism of fixed lividity. The fixed lividity was defined as an unfading phenomenon by thumb finger pressure. Skin specimens were taken from 68 autopsy cases 7.5-336 h (2 weeks) postmortem. Localization of Hb of the specimens was examined by a labeled streptabidin biotin (LSAB) method using polyclonal (rabbit antihuman hemoglobin antibody) and monoclonal (mouse anti-human hemoglobin monoclonal antibody) antibodies. Positive staining for Hb was observed in various sites of the skin, i.e. in only intravascular erythrocytes, in vascular walls and perivascular tissue including sweat glands and sebaceous glands, in the dermal connective tissue, and in almost all of skin tissue except the horny layer. The diffusion of Hb into skin tissue was observed in 20 of 41 displaceable lividity cases (49%) and 11 of 27 fixed lividity cases (41%). Compared to displaceable lividity, superficial plexi in fixed lividity were filled with erythrocytes, which were markedly immunodetected. These findings support the hypothesis that the fixation of lividity is not due to diffusion of Hb into skin tissue but hemoconcentration in blood vessels. Forensic Sci Int 1995 Apr 27;72(3):179-89
Penttila¿Í Laiho´Â »çüÀÇ ¸»ÃÊ Ç÷¾×¿¡¼ ´Ù¾çÇÑ ÇüÅÂÀÇ ¼¼Æ÷ ÇüŸ¦ ºÐ¼®ÇÏ¿´´Ù. ±× °á°ú´Â ´Ù¾çÇÑ Ç÷¾× ¼¼Æ÷ÀÇ ±¸Á¶¹°ÀÌ ÀÚ°¡¿ëÇ÷¿¡ »ó´çÇÑ ÀúÇ×¼ºÀÌ ÀÖ´Â °ÍÀ¸·Î ³ªÅ¸³µ´Ù.
The Estimation of the Time Since Death in the Early Postmortem Period, 1995, Edward Arnold; C Henssge, B Knight, T Krompecher; pp224
(ÂüÁ¶ 1)
1. ºÎÆеDZ⠽ÃÀÛÇϸé ÀûÇ÷±¸°¡ ±úÁö¸é¼ ³ª¿Â Çì¸ð±Û·ÎºóÀÌ Ç÷°üº®À» ºüÁ® ³ª¿Í Á¶Á÷¿¡ ħÂøµË´Ï´Ù. °ú°Å¿¡´Â ¾çÃø¼º ½Ã¹ÝÀ̳ª °íÁ¤ ½Ã¹ÝÀÌ »ý±â´Â ¿ø¸®¸¦ ¸ðµÎ ÀÌ°ÍÀ¸·Î ¼³¸íÇß¾ú½À´Ï´Ù.
2. Ç÷¾×Àº ÀûÇ÷±¸°¡ ¾à 45%À̸ç ÀϺΠ¹éÇ÷±¸¿Í ±âŸ °íÇü¼ººÐÀ» »©µµ ¾à 50%°¡ ¹°ÀÔ´Ï´Ù. »ç¸ÁÈÄ ÀÌ ¹°ÀÌ ¸ÕÀú Ç÷°üº®À» ºüÁ®³ª°¡¸é¼ ³óÃàÀÌ µÈ´Ù´Â °ÍÀÔ´Ï´Ù. ³óÃàÀÌ µÇ¸é µÉ¼ö·Ï Ç÷¾×ÀÇ À̵¿Àº ¹æÇØ¹Þ°Ô µË´Ï´Ù.
(ÂüÁ¶ 2)
Older theories about 'fixation' of the staining after a certain time are not tenable, as there is no constant interval when this occurs.
Formerly, it was held that if a body had remained in its original posture for a certain minimum length of time the blood would coagulate in the hypostatic areas, so that secondary shifting could not then occur if the body was moved. This is not true in the majority of instances, as there may be partial or complete secondary gravitation at any time- at least, until true staining of the tissue due to haemolysis begins as part of early decomposition, which is not until the second or third day in temperate conditions. Bernard Knight, Forensic Pathology, pp. 53
It may offer some indication as to whether the position of a body has been altered after it has become fixed(about 4 to 8 hours). Fracis E. Camps, Practical forensic medicine, pp.104
After 8 to 12 hours lividity becomes "fixed" and will remain where it originally formed. Simpson and Knight, Forensic Medicine pp. 9
After about 10-12 hours the lividity becomes "fixed" and repositioning the body, e.g. from the prone to the supine position, will result in a dual pattern of lividity since the primary distribution will not fade completely. Fixation of lividity is a relative, rather than an absolute, phenomenon, but nevertheless, well developed lividity fades very slowly and only incompletely. Duality of the distibution of lividity is important because it shows that the body had been moved after death. However, the timing of this movement of the body is inexact. Prof. Derrick J. Pounder.
After 4-5 days the ever-increasing haemolysis in the vessels produces sufficent pigment to stain the hypostatic areas, and this is permanent. Gradwohl's legal medicine pp.81
(ÂüÁ¶ 3)
Autolytic changes in blood cells of human cadavers. II. Morphological studies.
The morphology of various types of cells in the peripheral blood of human cadavers was investigated. The material comprised 123 medicolegal autopsy cases with post-mortem (p.m.) times ranging fro 1.7 to 270.4 hours. The corpses were kept at +4 degrees C. The haematocrit values of the blood increased rapidly after death. The haematocrit-corrected red cell count, and the total white cell and platelet counts remained quite stable during the whole p.m. time range. Red cells were quite rapidly transformed from a discoid configuration to crumbled discs, echinocytes and spherocytes, but no debris or burst cell configurations were seen. Rapid deterioration of the staining properties and marked morphological changes in many leucocytes occurred quite rapidly after death. Lymphocytes seemed to be the most resistant and basophils the least resistant to the effects of autolysis. Morphologically altered platelets and aggregates of them were seen in each cadaver. The present morphological observations and the quantitative results suggest that various cellular elements of the blood seem to be quite resistant to autolytic effects, and many cells apparently retain their viability for longer periods of time in the blood of cadavers kept at reduced temperature. Penttila A, Laiho K.; Forensic Sci Int 1981 Mar-Apr;17(2):121-32
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