| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8952812 | The Egyptian Journal of Radiology and Nuclear Medicine | 2018 | 4 Pages |
Abstract
Placental site trophoblastic tumor is a very rare neoplasm and is a subtype of gestational trophoblastic neoplasm. Owing to its rarity and varied clinical manifestations, it can lead to a diagnostic dilemma. We report a very rare case of PSTT presenting as massive hemoperitoneum caused by rupture of secondary arteriovenous malformation. MR angiogram revealed the presence of arteriovenous malformation and the diagnosis of the neoplasm was confirmed on histopathology and immunohistochemistry. Hysterectomy was done and the patient was managed successfully.
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Authors
Avantika Gupta, Usha Manaktala, Nita Khurana,