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  Vol. 78 No. 1, January 1959 TABLE OF CONTENTS
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Retroperitoneal Lymphangioma

ROBERT F. RAUCH, M.D.

AMA Arch Surg. 1959;78(1):45-50.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

Lymphangioma has been called the rarest of tumors found in the retroperitoneal region. Only isolated case reports of cavernous or cystic retroperitoneal lymphangiomas have been seen.1-4,7-13,15,17-21 I am reporting two cases of retroperitoneal cystic lymphangioma because of the rarity of the lesion. A review of the literature of all previously recorded cases of retroperitoneal lymphangioma has been added to acquaint the general surgeon, urologist, and gynecologist with the clinical findings of this condition.

Report of Cases

CASE 1.

—A 17-year-old sheet-metal worker entered Mount Carmel Hospital on July 10, 1955, complaining of nausea, vomiting, and generalized abdominal pain of 14 hours' duration. The colicky pain increased with activity and defecation. The past history was negative.

Physical examination disclosed a well-developed. well-nourished youth who appeared acutely ill. The temperature was 100.2 F, pulse 92, B. P. 114/80, and respirations 24. Physical examination was essentially normal except for muscle spasm throughout . . . [Full Text PDF of this Article]


Author Affiliations

Columbus, Ohio

From the Department of Surgery, Ohio State University College of Medicine.


Footnotes

Submitted for publication July 23, 1958.



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