TY - JOUR
T1 - Adrenal intravascular papillary endothelial hyperplasia
AU - Holmes, Casey
AU - Akhras, Anwar
AU - Schneider, Andrew
AU - Yacoub, Joseph H.
AU - Picken, Maria
AU - Kabaker, Adam
N1 - Publisher Copyright:
© 2017, Jaypee Brothers Medical Publishers (P) Ltd. All rights reserved.
PY - 2017
Y1 - 2017
N2 - Aim: We describe the rare case of a woman with adrenal intravascular papillary endothelial hyperplasia (IPEH) or Masson’s tumor. We present relevant background information on IPEH and our case report, as well as describe a workup and treatment plan for the lesion. Introduction: Intravascular papillary endothelial hyperplasia (IPEH) or Masson’s tumor is a rare lesion, i.e., predominantly found in the oral cavity, head, and neck.1-4 To our knowledge, only six adrenal IPEH cases have been reported in the literature to date.4 Case report: A 49-year-old woman originally presented to us with an incidentaloma found on computed tomography scan. Due to the eventual size increase of the mass, a laparoscopic left adrenalectomy was performed. Pathologic evaluation of the mass revealed a 3 cm IPEH arising in a hemangioma within the adrenal gland. Conclusion: Before the diagnosis of IPEH is considered as the etiology for an adrenal incidentaloma, it is crucial to rule out more common tumors. Serological and radiographic studies are critical to the workup. Clinical Significance: The IPEH is a very interesting lesion of the adrenal gland, however, it is exceedingly rare and thus exclusion of more common and serious lesions must be done prior to the diagnosis of IPEH.
AB - Aim: We describe the rare case of a woman with adrenal intravascular papillary endothelial hyperplasia (IPEH) or Masson’s tumor. We present relevant background information on IPEH and our case report, as well as describe a workup and treatment plan for the lesion. Introduction: Intravascular papillary endothelial hyperplasia (IPEH) or Masson’s tumor is a rare lesion, i.e., predominantly found in the oral cavity, head, and neck.1-4 To our knowledge, only six adrenal IPEH cases have been reported in the literature to date.4 Case report: A 49-year-old woman originally presented to us with an incidentaloma found on computed tomography scan. Due to the eventual size increase of the mass, a laparoscopic left adrenalectomy was performed. Pathologic evaluation of the mass revealed a 3 cm IPEH arising in a hemangioma within the adrenal gland. Conclusion: Before the diagnosis of IPEH is considered as the etiology for an adrenal incidentaloma, it is crucial to rule out more common tumors. Serological and radiographic studies are critical to the workup. Clinical Significance: The IPEH is a very interesting lesion of the adrenal gland, however, it is exceedingly rare and thus exclusion of more common and serious lesions must be done prior to the diagnosis of IPEH.
KW - Adrenal tumor
KW - Adrenalectomy
KW - Case report
KW - Laparoscopic
UR - http://www.scopus.com/inward/record.url?scp=85020453134&partnerID=8YFLogxK
U2 - 10.5005/jp-journals-10002-1201
DO - 10.5005/jp-journals-10002-1201
M3 - Article
AN - SCOPUS:85020453134
VL - 9
SP - 16
EP - 19
JO - World Journal of Endocrine Surgery
JF - World Journal of Endocrine Surgery
SN - 0975-5039
IS - 1
ER -