SPONTANEOUS RUPTURE OF T H E PATHOLOGIC SPLEEN REPORT OP TWO UNUSUAL CASES* WILLIAM ARONSON AND ROBERT A. POX From the Department of Pathology, Morrisania City Hospital, New York City Schmidt 1 found that rupture of the spleen was fifteen times more common in 1932 than it was in 1913. He pointed out that between 1913 and 1926 he saw about two cases each year, whereas between 1926 and 1932 he saw approximately thirty-two cases each year. No doubt this marked increase in splenic rupture is partially due to increased automobile and airplane travel as well as to more frequent recognition of the condition by the medical profession. We report two cases of spontaneous rupture of the pathologic spleen admitted to the Morrisania City Hospital within thirteen days. The first case is one of spontaneous rupture of a splenic hemangioma. The second case followed mild trauma in an unsuspected case of leukemia. Case 1. J. 0., aged 36, white German male admitted 8/25/39 with a history of abdominal pain. Four days prior to admission the patient began to have intermittent colicky abdominal pain localized to the left upper quadrant, moderately severe in character, and unrelated to the ingestion of food. Catharsis resulted in a watery diarrhea of two days duration followed by constipation. Twelve hours before admission two enemas were successful. Stools were never bloody or tarry. Immediately following the enemata he experienced a severe stabbing, constant, non-radiating left upper quadrant pain which caused him to seek hospitalization. Just before admission he fainted while at stool. The patient gave an indefinite history of pneumonia and a fall from a building in 1927 sustaining no serious injury. Physical examination revealed a well-developed, well-nourished adult male in shock. Temperature 102.6 degrees, pulse imperceptible. Thefindingswere localized to the abdomen which was slightly protuberant but not tympanitic. * Received for publication January 30, 1940. 868 SPONTANEOUS R U P T U R E OF SPLEEN 869 There was marked muscle guarding in the upper quadrants, particularly on the left, associated with considerable tenderness in the left upper quadrant and left lumbar region. No costovertebral angle tenderness, palpable masses or viscera. Stools were light brown in color. Hemoglobin 75 per cent (Sahli), R.B.C. 4.2M per cu. mm., W.B.C. 19,000 per cu. mm., polymorphs 88 per cent lymphocytes 12 per cent. A flat plate of the abdomen showed no free air beneath the diaphragm. Electrocardiogram showed a sinus tachycardia of 166 per minute. Diagnoses of acute pancreatitis, abdominal hemorrhage and FIG. 1. SPLENIC CAVERNOUS HEMANGIOMA Arrow indicates rupture mesenteric thrombosis were considered. Because of the poor condition of the patient, surgery was deferred and shock therapy was instituted, but he failed to respond and died 5 hours following admission. At autopsy the abdomen was found to be filled with approximately 2000 cc. of bright red blood, the source of which was a ragged tear in the capsule at the lower pole of the spleen. The remaining viscera were normal. The spleen was the usual deep red-blue color of shock, measuring 12 x 6 x 3 cm. and weighing 360 gms. At the lower pole a ruptured hemangioma, 1 cm. in diameter, was 870 WILLIAM ARONSON AND ROBERT A. FOX located from which the hemorrhage had apparently occurred (fig. 1), burrowing its way beneath the capsule to form a V on the superior surface. Microscopic examination: Sections from the bleeding area revealed a ruptured capsule surrounded by a polymorphonuclear cell reaction. This area was devoid of splenic tissue and in its place thin-walled cavernous sinuses filled with non-clotted blood were found (fig. 2). F I G . 2. CAVERNOUS SINUSOIDS CONTAINING UNCLOTTBD BLOOD Case 2. A. L., aged 11, white Hebrew male, admitted 9/7/39 with a history of epigastric pain of one hour duration. The patient received a mild blow to the abdomen, administered by a playmate, which caused him to fall; no apparent injury was sustained. After several minutes he returned to his home because he did not feel well and where his father found him one-half hour later lying in bed looking very pale. Upon attempting to visit the bathroom unassisted he fainted and remained unconscious for a few seconds. Because of increasing abdominal pain, hospitalization was deemed advisable. Past history was non-contributory except for chiokenpox in 1929, tonsillectomy in 1935 and measles in 1939. Physical examination revealed a well developed white male child weighing SPONTANEOUS R U P T U R E OF S P L E E N 871 V,>. F I G . 3. ENLARGED LEUKEMIC SPLEEN; SMOOTH GRAY SURFACE RUPTURED ABEA F I G . 4. SPLENIC V E I N SHOWING MANY MYELOBLASTS SHOWING 872 WILLIAM ARONSON AND ROBERT A. POX 110 lbs., in shock. Temperature 100.4 degrees, pulse 140 per minute, respirations 42 per minute. Lungs were clear and the heart sounds were normal but rapid. The upper quadrants of the abdomen were moderately rigid. The liver and spleen could not be palpated. The testes were undescended. There was no lymphadenopathy. R.B.C. 4.3M per cu. mm., W.B.C. 65,800 per cu. mm., polymorphs 38 per cent, small and large mononuclears 62 per cent. Diagnosis was ruptured spleen and an immediate operation was performed. The abdominal cavity was rilled with free blood and clots. The capsule of the spleen had been torn and blood was oozing from several lacerations in the splenic substance. The spleen was enlarged. A splenectomy was done but in spite of several blood transfusions and supportive therapy the patient expired 12 hours following operation. At autopsy no tracheo-bronchial or mesenteric lymphadenopathy, or other pathology was found. The spleen weighed 400 grams and measured 15 x 10 x 4 cm. (upper limits normally are 12 x 7 x 3 cm.) 2 . I t was grayish-red in color and appeared to be extremely engorged. A tear through the capsule into the parenchyma at the lower pole, 2 x 1 cm., was found. The consistency was moderately firm (fig. 3). The cut surface was gray in appearance and congested; the substance of the parenchyma was extremely friable. Microscopic examination: The histopathology was that of a myeloid leukemia. The myeloblasts were seen to be growing diffusely and crowded the red pulp to the point where they had replaced the lymphocytes of the Malphigian corpuscles, giving rise to a uniform cellular appearance. The pulp also contained red blood cells, lymphocytes, less numerous polymorphonuclears, large monocytic cells and reticulo-endothelial cells of the stroma. Broken down hemoglobin was also present some of which was intracellular but much more was extracellular (fig. 4). SUMMARY Two cases of rupture of the spleen are reported because of the totally unsuspected underlying pathology. Although the literature is replete with case reports of rupture of normal and malarial spleens, we found that leukemic spleens are only rarely known to rupture, and were unable to find any previous report of spontaneous rupture of a splenic hemangioma. REFERENCES (1) MAINGOT, RODNEY: Postgraduate Survey. Vol. 1, Part 2, page pages 232, 245. W. Blakiston's Sons & Co., Philadelphia, 1929. 890. D. Appleton-Century Co., (4) DELAFIBLD AND PRUDDEN: Text- 1937. (2) GRAY, H.: Anatomy of the Human Body. Lea and Febriger, Phila., 1930, page 1277. (3) KAUFMAN, E.: Pathology. Vol.1-, Book of Pathology. 11th Edition, page 567, William Wood and Company. (5) DOWD, C. N.: Angioma of the spleen. Ann. Surg., 62:177,1915.
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