scholarly journals A case report of idiopathic hyperaldosteronism characterized by bilateral adrenal adenoma

Medicine ◽  
2019 ◽  
Vol 98 (43) ◽  
pp. e17418
Author(s):  
Wei Wang ◽  
Feng Wei ◽  
RanHao Li ◽  
JiaHui Tian
2011 ◽  
pp. P1-593-P1-593
Author(s):  
Hans K Ghayee ◽  
Aliya S Heyliger ◽  
Stacey Woodruff ◽  
Fiemu E Nwariaku ◽  
Richard J Auchus

2019 ◽  
Vol 4 (3) ◽  

Intravascular Papillary Endothelial Hyperplasia (IPEH) or Masson’s Tumor is a benign vascular tumor, most commonly seen on the skin and usually on the head, neck or extremities. It is more common in women with no age predilection. Visceral involvement is very rare, with about 30 intra-abdominal reports. We present a case report of a 58 year old woman who underwent a CT scan due to dysphagia complaints, with an incidental known finding of growth in the adrenal adenoma, which was 5 cm in diameter on hospitalization. The patient underwent laparoscopic adrenalectomy. Biopsy results demonstrated a brownish yellow lesion, 2.8 cm in diameter, composed of a blood clot and septate. Immunochemical staining for CD31 and CD34 was positive and the lesion was diagnosed as an IPEH of pure form. Our review of literature examines different forms of IPEH, previous reports and characteristics of Masson’s tumors in the adrenal gland and stratifies ways of differentiation it from other benign or malignant lesions of the adrenal.


Cases Journal ◽  
2009 ◽  
Vol 2 (1) ◽  
pp. 7965 ◽  
Author(s):  
Jeremiah T Martin ◽  
Fuad Alkhoury ◽  
Scott Helton ◽  
Paul Fiedler ◽  
Olga Sakharova ◽  
...  

2018 ◽  
Vol 44 ◽  
pp. 118-121
Author(s):  
Shiro Matsumoto ◽  
Yoshinori Hosoya ◽  
Alan Kawarai Lefor ◽  
Hidenori Haruta ◽  
Takashi Ui ◽  
...  

2003 ◽  
Vol 44 (2) ◽  
pp. 158-159 ◽  
Author(s):  
K. Chelaifa ◽  
K. Bouzaidi ◽  
S. Chouaib ◽  
O. Azaiz ◽  
M. Ben Messaoud ◽  
...  

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Mohammad Hossein Anbardar ◽  
Neda Soleimani ◽  
Saman Nikeghbalian ◽  
Maryam Mohebbi

Abstract Background Adrenal incidentalomas are often found during investigation for another tumor or unrelated problems. Except for adrenal myelolipoma (second most common primary adrenal incidentaloma following adrenocortical adenomas), adrenal lipomatous tumors are uncommon generally and are often described as case reports in the literature. Since the amount of fat is variable, without the help of advanced imaging techniques, some adrenal lipomatous tumors may be misdiagnosed before pathologic examination. Herein, we report a case of adrenal adenoma with myelolipomatous metaplasia that was excised as a periceliac mass in the setting of recurrent pancreatic cyst. Case report A 45-year-old Iranian woman with hypertension and end-stage renal disease presented with recurrence of a pancreatic cyst (previous pathologic report was mucinous cyst adenoma). During exploratory laparotomy, the mentioned pancreatic cyst was tightly attached to the stomach and jejunum. There was also a periceliac round rubbery lesion (firstly diagnosed by endoscopic ultrasound) that was excised for ruling out malignancy. Histologic examination of the periceliac mass was found to be adrenocortical adenoma with foci of myelolipomatous metaplasia. The pancreatic cyst histology was just a pseudocyst. Conclusion Our case highlights the significance of complete evaluation of incidental findings before surgical intervention, even in the setting of another primary tumor. Myelolipoma and myelolipomatous change (metaplasia) are two different entities. Although very similar as to pathogenesis, there are still some differences.


2017 ◽  
Author(s):  
Marta Kialka ◽  
Tomasz Milewicz ◽  
Katarzyna Doroszewska ◽  
Sandra Mrozinska ◽  
Robert Jach

2014 ◽  
Vol 37 (10) ◽  
pp. e169 ◽  
Author(s):  
C. Virevialle ◽  
E. Brasnu ◽  
R. Fior ◽  
C. Baudouin

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