Vol 73, No 6 (2023)
Pictures in Oncology
Published online: 2023-10-16

open access

Page views 464
Article views/downloads 287
Get Citation

Connect on Social Media

Connect on Social Media

The diagnostic dilemma of low-grade adrenal cortical carcinoma in a young female patient

Maciej D. Bugajski1, Agata Popow-Gierba1, Małgorzata Wysocka-Malik1
Nowotwory. Journal of Oncology 2023;73(6):404.

Abstract

Not available

Pictures in oncology

NOWOTWORY Journal of Oncology

2023, volume 73, number 6, 404

DOI: 10.5603/njo.96782

© Polskie Towarzystwo Onkologiczne

ISSN 0029–540X, e-ISSN: 2300-2115

www.nowotwory.edu.pl

The diagnostic dilemma of low-grade adrenal cortical carcinoma in a young female patient

Maciej D. Bugajski Agata Popow-GierbaMałgorzata Wysocka-Malik
Department of Radiology and Diagnostic Imaging, Maria Sklodowska-Curie Institute of Oncology, Krakow Branch, Krakow, Poland

How to cite:

Bugajski MD, Popow-Gierba A, Wysocka-Malik M. The diagnostic dilemma of low-grade adrenal cortical carcinoma in a young female patient. NOWOTWORY J Oncol 2023; 73: 404.

This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially.

A 33-year-old woman with hypertension and oligomenorrhea for last 6 months, with an incidentally diagnosed abdominal mass on ultrasound underwent an MRI and 18F-FDG PET-CT (fig. 1, 2). No abnormalities were seen on lab tests. Initial diagnoses were ganglioneuroma, adrenal cortical carcinoma (ACC) and pheochromocytoma. Ganglioneuroma was supported by age, normal/lower level of adrenal hormones, well-circumscribed margins, progressive enhancement and persistent in delayed phase (in T1w before and after dynamic administration of gadobutrol) and no evidence of metastasis [1, 2]. ACC was supported by haemorrhage on T1w, heterogeneous T2w signal – higher than an adjacent liver, enhanced density of periadrenal fat [1, 2]. Pheochromocytoma was less confident due to the relatively low signal on T2w. High FDG uptake (SUVmax 9.0) suggested a malignant character. For all diagnosis parameters like lesion size (11 cm), there was no presence of drop of signal during out-of-phase sequence, no evidence of IVC invasion and local compressive symptoms showed imaging overlap [1, 2]. DWI revealed a high signal within the lesion, with a low signal on ADC maps. However, DWI does not help a lot in malignant/benign adrenal lesion differentiation [2]. ACC is a very rare and aggressive malignancy, with annual incidence 0.5–2 cases/ million [2]. Excision is a primary treatment for stage I–III disease with adjuvant therapy due to high risk of recurrence even with complete resection [2]. In this case, PET-CT showed adrenal/liver SUV ratio >1.8, indicating the malignant character of the lesion [2]. On laparotomy low-grade ACC, Weiss score 5, Ki-67: 11% was confirmed.

Figure 1. MRI, T2-weighted image showing 11cm oval, well-circumscribed mass with high, heterogeneous signal, higher than the adjacent liver
Figure 2. Fluorine-18F-FDG-PET-CT PET-CT scan indicating high FDG uptake (SUV max 9.0), more than 3 times higher than the adjacent liver

References

  1. Shawa H, Elsayes K, Javadi S, et al. Adrenal ganglioneuroma: features and outcomes of 27 cases at a referral cancer centre. Clin Endocrinol. 2013; 80(3): 342–347, doi: 10.1111/cen.12320.
  2. Ahmed AA, Thomas AJ, Ganeshan DM, et al. Adrenal cortical carcinoma: pathology, genomics, prognosis, imaging features, and mimics with impact on management. Abdom Radiol (NY). 2020; 45(4): 945–963, doi: 10.1007/s00261-019-02371-y, indexed in Pubmed: 31894378.