A Rare Presentation of Adrenocortical Carcinoma-Spontaneous Rupture with Sub capsular Splenic Hematoma

Journal Title: Scholars Journal of Medical Case Reports - Year 2015, Vol 3, Issue 10

Abstract

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with an incidence rate of 1 to 2 per million. Clinical symptoms are mainly related to an excess of steroid hormones or tumor bulk. The most common metastatic sites are the liver, lungs, lymph nodes and bone. Surgical resection remains the cornerstone of treatment. The case mentioned here has two rare characteristics. First that spontaneous rupture of ACC is very rare and secondly associated splenic sub capsular hematoma has never been reported. A 63 year old non-hypertensive male presented in the emergency department with the complaints of pain and gradually increasing lump in the left side of abdomen since last 3 months. On initial clinical examination he was diagnosed to have splenomegaly by emergency medical officer. USG showed to have splenomegaly and left suprarenal mass lesion for which he was referred to urology department. CECT of abdomen revealed heterogeneously enhancing left adrenal ruptured mass lesion with involvement of left kidney and large splenic sub capsular hematoma (13.8x3.2x14.8cms). CEMR findings correlated to CECT. Serum cortisol and urinary metanephrines were normal. Patient was planned for surgery and intraoperatively was found to have locally extensive adrenal tumor with large sub capsular splenic hematoma with left kidney involvement. Adrenalectomy, nephrectomy and splenectomy was done with the palliative intent which relieved patient symptomatically. HPE of specimen showed it to be adrenocortical carcinoma. Though spontaneous rupture of pheochromocytoma and cysts is reported in literature, to our knowledge this is the first reported case of spontaneous adrenocortical carcinoma rupture with sub capsular splenic hematoma. Keywords: Adrenocortical carcinoma, Spontaneous rupture, splenic hematoma, Adrenalectomy, Nephrectomy.

Authors and Affiliations

Rajeev T. P, Nitin Gupta, Debanga Sarma, Sasanka K. Barua

Keywords

Related Articles

The Double Aortic Arch: About Two Cases and Literature Review

The double aortic arch is a rare embryological anomaly; it constitutes < 1% of all congenital heart defects. It leads to the formation of a complete vascular ring encircling the tracheo-esophageal axis, causing respirato...

Multiple Episodes of Upper Gastrointestinal Bleeding Revealing a Splenic Artery Aneurysm

The aneurysm of the splenic artery is a rare entity. the diagnosis is not always easy, because of the nonspecific symptomatology. We present the case of a 68-year-old woman treated for splenic artery aneurysm (SAA), who...

Late Onset Joubert Syndrome: Case Report

Joubert Syndrome (JS) is a rare congenital autosomal recessive disorder. Obligatory finding and Hallmark feature is Molar tooth sign, a complex midbrain hindbrain malformation visible on MRI brain. Cardinal clinical feat...

Atypical Presentation of Giant Hepatic Sol in a Three Years Old Girl

We report a case of three years old female child presenting with giant abdominal SOL eventually diagnosed as benign hepatic mass. The size of the lesion with its way of presentation is a rare entity in this age group. K...

Using Antibiotic loaded bone cement (ALBC) as the novel method to treatment of chronic osteomyelitis

Bone and joint infection is the main complication of bone fracture as a result of pyogenic bacteria. The long-term clinical course, extended period of silence, cases of recurrence and abundant discharge are the overridin...

Download PDF file
  • EP ID EP377085
  • DOI -
  • Views 89
  • Downloads 0

How To Cite

Rajeev T. P, Nitin Gupta, Debanga Sarma, Sasanka K. Barua (2015). A Rare Presentation of Adrenocortical Carcinoma-Spontaneous Rupture with Sub capsular Splenic Hematoma. Scholars Journal of Medical Case Reports, 3(10), 998-1001. https://europub.co.uk/articles/-A-377085