Adrenocortical Tumor Presenting As Hemoperitonium - A Rare Case

Dr Ramesh Kumar Korumilli, Dr Jakkula Srikanth, Dr Raheemuddin Khan, Dr Sri Harsha Muvva

Abstract: Adrenocortical carcinomas are rare malignancies, which can present with diverse clinical manifestations. They can be functional, i. e. , hormone secreting tumors or non-functional. In cases of hormone-secreting tumors, the hormone in excess determines the diagnostic clinical presentation. On the other hand, biologically inert tumors are diagnosed either due to their mass effect or as incidental findings. A very few present as a result of their potentially life-threatening complications. We present here a case of a 28-year-old female patient who underwent emergency laparotomy due to signs of acute abdomen and concomitant cardiovascular collapse caused by a spontaneously ruptured left adrenocortical carcinoma. The patient was operated for that and left adrenalectomy with splenectomy was performed where the tumor was removed in toto.

Keywords: adrenocortical, haemoperitonium, tumor markers,

How to Cite?: Dr Ramesh Kumar Korumilli, Dr Jakkula Srikanth, Dr Raheemuddin Khan, Dr Sri Harsha Muvva, "Adrenocortical Tumor Presenting As Hemoperitonium - A Rare Case", Volume 7 Issue 1, January 2018, International Journal of Science and Research (IJSR), Pages: 1467-1470, https://www.ijsr.net/getabstract.php?paperid=ART20179656, DOI: https://dx.doi.org/10.21275/ART20179656