Splenic rupture as the presenting manifestation of primary splenic angiosarcoma in a teenage woman: a case report
IntroductionPrimary splenic angiosarcoma is a rare neoplasm of vascular origin carrying a very poor prognosis, partly due to its high metastatic potential. This disease presents frequently with splenic rupture and hemorrhage.
We report the case of a 17-year-old woman who presented with rupture of a primary splenic angiosarcoma.Case presentationThe patient presented with diffuse abdominal pain and distention. Clinical examination revealed severe tenderness in the left upper abdominal quadrant, a palpable abdominal mass, and hemodynamic instability with a systolic arterial blood pressure of 75mmHg and heart rate of 135 beats per minute.
Blood tests revealed anemia (hemoglobin 7.0g/dl) and thrombocytopenia (platelets 70x109/liter). After initial fluid resuscitation and stabilization, abdominal ultrasound and computed tomography were performed, revealing a large quantity of intraperitoneal free fluid, an enlarged spleen, and a heterogeneous low-density signal within the splenic parenchyma, which showed varying degrees of contrast enhancement.
At laparotomy a huge (weight 1530g, diameter 19cm) actively bleeding spleen was identified and splenectomy was performed. Histopathology showed a primary splenic angiosarcoma.
After an uneventful recovery, the patient was discharged on the sixth postoperative day.
Conclusions: Primary splenic angiosarcoma is rare. Although this malignancy is usually encountered in advanced age, there have been a few reported cases among younger patients.
The case reported here presented with splenic rupture, was treated by laparotomy and splenectomy, and the patient is disease free 16 months after surgery.
Author: Andreas Manouras, Panagiotis Giannopoulos, Levon Toufektzian, Haridimos Markogiannakis, Emmanuel E Lagoudianakis, Artemisia Papadima, Dimitrios Papanikolaou, Konstantinos Filis and Panagiotis Kekis
Credits/Source: Journal of Medical Case Report
Published on: 2008-04-29
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