Cystic adrenal lesions: focus on pediatric population (a review)

Authors

  • Mara Carsote
  • Adina Ghemigian
  • Dana Terzea
  • Adina-Augusta Gheorghisan-Galateanu
  • Ana Valea

DOI:

https://doi.org/10.15386/cjmed-677

Keywords:

adrenal cyst, adrenal hemorrhage, cystic neuroblastoma

Abstract

Background and aim

The cysts may potentially affect any organ; adrenals cysts are rare. This is a review of the literature regarding adrenal cysts, focusing on children and young adults.

General data

Three major types have been described: pure cysts (endothelial, epithelial, and hemorrhagic or pseudocyst), parasitic (as hydatid) cysts and cystic part of a tumour (most frequent are neuroblastoma, ganglioneuroma, pheocromocytoma, and teratoma). The complications are: bleeding, local pressure effects; infection; rupture (including post-traumatic); arterial hypertension due to renal vessels compression. Adrenal hemorrhage represents a particular condition associating precipitating factors such as: coagulation defects as Factor IX or X deficiency, von Willebrand disease, thrombocytopenia; antiphospholipid syndrome; previous therapy with clopidogrel or corticosteroids; the rupture of a prior tumour. At birth, the most suggestive features are abdominal palpable mass, anemia, and persistent jaundice. Adrenal insufficiency may be found especially in premature delivery. The hemorrhage is mostly self-limiting. Antenatal ultrasound diagnosis of a cyst does not always predict the exact pathology result. The most important differential diagnosis of adrenal hemorrhage/hemorrhagic cyst is cystic neuroblastoma which is highly suggestive in the presence of distant metastases and abnormal catecholamine profile. The major clue to differentiate the two conditions is the fact that the tumor is stable or increases over time while the adrenal hemorrhage is expected to remit within one to two weeks.

Conclusion

Pediatric adrenal cysts vary from simple cysts with a benign behavior to neoplasia- related lesions displaying severe prognosis as seen in cystic neuroblastoma. A multidisciplinary team is required for their management which is conservative as close follow-up or it makes necessary different surgical procedures in cases with large masses or if a malignancy suspicion is presented. Recently, laparoscopic approach is regarded as a safe procedure by some authors but generally, open surgery is more frequent used compare to adults; in most cases the preservation of normal gland is advisable.

Author Biographies

Mara Carsote, C.Davila University of Medicine and Pharmacy & C.I.Parhon National Institute of Endocrinology, Bucharest, Romania

Endocrinology

Adina Ghemigian, C.Davila University of Medicine and Pharmacy & C.I.Parhon National Institute of Endocrinology, Bucharest, Romania

Endocrinology

Dana Terzea, Monza Oncoteam Hospital & C.I.Parhon National Institute of Endocrinology, Bucharest, Romania

Endocrinolgy

Adina-Augusta Gheorghisan-Galateanu, .C.Davila University of Medicine and Pharmacy & C.I.Parhon National Institute of Endocrinology, Bucharest, Romania

Endocrinology

Ana Valea, I.Hatieganu University of Medicine and Pharmacy & Clinical County Hospital, Cluj-Napoca, Romania

Endocrinology

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Published

2017-01-30

How to Cite

1.
Carsote M, Ghemigian A, Terzea D, Gheorghisan-Galateanu A-A, Valea A. Cystic adrenal lesions: focus on pediatric population (a review). Med Pharm Rep [Internet]. 2017 Jan. 30 [cited 2025 Oct. 6];90(1):5-12. Available from: https://medpharmareports.com/index.php/mpr/article/view/677

Issue

Section

Reviews