Radiological differentiation of phaeochromocytoma from other malignant adrenal masses: importance of wash-in characteristics on multiphase CECT.

multiphase CECT peak arterial enhancement percentage arterial enhancement phaeochromocytoma

Journal

Endocrine connections
ISSN: 2049-3614
Titre abrégé: Endocr Connect
Pays: England
ID NLM: 101598413

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 20 05 2019
accepted: 05 06 2019
entrez: 29 6 2019
pubmed: 30 6 2019
medline: 30 6 2019
Statut: ppublish

Résumé

To evaluate the computerised tomography (CT) characteristics of phaeochromocytoma (PCC) that differentiate them from other non-benign adrenal masses such as adrenocortical carcinoma (ACC), primary adrenal lymphoma (PAL) and adrenal metastases (AM). This retrospective study was conducted at a tertiary health care institute from Western India. Patients presented between January 2013 and August 2016 with histological diagnosis of PCC or other non-benign adrenal mass having adequate reviewable imaging data comprising all four CECT phases were included. The study cohort consisted of 72 adrenal masses from 66 patients (33 PCC, 22 ACC, 4 PAL, 13 AM). Unlike other masses, majority of PCC (25/33) showed peak enhancement in early arterial phase (EAP). PCC had significantly higher attenuation in EAP and early venous phase (EVP), and higher calculated percentage arterial enhancement (PAE) and percentage venous enhancement (PVE) than other adrenal masses (P < 0.001). For diagnosis of PCC with 100% specificity, PAE value ≥100% and EAP attenuation ≥100 HU had 78.8 and 63.6% sensitivity respectively. ACC were significantly larger in size as compared to PCC and metastasis. The adreniform shape was exclusively found in PAL (two out of four) and AM (4 out of 13). None of the enhancement, wash-in or washout characteristics were discriminatory among ACC, PAL and AM. Peak enhancement in EAP, PAE value ≥100% and EAP attenuation ≥100 HU differentiate PCC from other malignant adrenal masses with high specificity.

Identifiants

pubmed: 31252396
doi: 10.1530/EC-19-0198
pii: EC-19-0198
pmc: PMC6599213
doi:
pii:

Types de publication

Journal Article

Langues

eng

Pagination

898-905

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Auteurs

Manjunath Goroshi (M)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.
Jawaharlal Nehru Medical College, Belagavi, India.

Swati S Jadhav (SS)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Vijaya Sarathi (V)

Narayana Medical College and Hospital, Nellore, Andhra Pradesh, India.

Anurag R Lila (AR)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Virendra A Patil (VA)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Ravikumar Shah (R)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Priya Hira (P)

Department of Radiology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Rajaram Sharma (R)

Department of Radiology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Shettepppa Goroshi (S)

Department of Radiology, Sri Nijalingappa Medical College Bagalkot, Navanagar, Karnataka, India.

Gwendolyn Fernandes (G)

Department of Pathology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Amey Rojekar (A)

Department of Pathology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Abhay Dalvi (A)

Departments of General Surgery, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Ganesh Bakshi (G)

Department of Uro-Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India.

Gagan Prakash (G)

Department of Uro-Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India.

Nalini S Shah (NS)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Tushar R Bandgar (TR)

Department of Endocrinology, Seth GS Medical College and KEM Hospital, Parel, Mumbai, India.

Classifications MeSH