Evidence map›Paper›PMID 42700419›Full record

ArticleHormone research in paediatrics2026

Novel Insights Large Estrogen and Cortisol Co-Secreting Adrenocortical Tumor in a 17-Year-Old Female: A Case Report and Literature Review.

Simrat Kaur Veera, Nitsan Shacham, Jessy Epstein, Danielle Wolfe Cohen, Elizabeth Roman, Kristen M Thomas, Marissa Lipton, Brenda Kohn

Abstract readCase Reports
In one paragraph

Article in Hormone research in paediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Simrat Kaur VeeraDivision of Pediatric Endocrinology, NYU Grossman School of Medicine, New York, USA, simrat.veera@gmail.com.
Nitsan ShachamDivision of Pediatric Endocrinology, NYU Grossman School of Medicine, New York, USA.
Jessy EpsteinDivision of Pediatric Endocrinology, NYU Grossman School of Medicine, New York, USA.
Danielle Wolfe CohenDivision of Pediatric Hematology/Oncology, NYU Grossman School of Medicine, New York, USA.
Elizabeth RomanDivision of Pediatric Hematology/Oncology, NYU Grossman School of Medicine, New York, USA.
Kristen M ThomasDivision of Pathology, NYU Grossman School of Medicine, New York, USA.
Marissa LiptonDivision of Pediatric Nephrology, NYU Grossman School of Medicine, New York, USA.
Brenda KohnDivision of Pediatric Endocrinology, NYU Grossman School of Medicine, New York, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAdrenocortical tumors (ACTs) are rare pediatric tumors which include both benign adrenocortical adenomas (ACAs) and malignant adrenocortical carcinomas (ACCs). The most common presentations of an ACT in children are virilization and/or Cushing's syndrome resulting from tumoral secretion of androgens and cortisol, respectively. Adrenocortical tumors that express high levels of estrogen are extremely rare, and adrenal tumors that co-secrete more than one class of adrenal hormones raise concern for malignancy. CASE PRESENTATION: We present a case of a 17-year-old female presenting with weight gain, secondary amenorrhea, and acute abdominal pain. She was found to have a large (9.4 cm) right adrenal tumor co-secreting both cortisol and estrogen, which was successfully surgically removed by minimally invasive laparoscopy. Her perioperative course was complicated by severe refractory hypertension requiring multiple antihypertensive medications, and venous thromboses associated with hypercoagulability. Genetic testing revealed no germline driver mutation. Classification of the adrenal tumor as either benign or malignant was discordant when determined by the adult Weiss vs. the pediatric AFIP/Wieneke criteria in this older adolescent.

conclusionThis prismatic case of a rare estrogen-cortisol secreting tumor raises discussion regarding the complexities in the clinical presentation and uncertainties in prognosis of adrenal tumors in adolescents. A literature review showcases 19 case reports published between 1948 and 2025 of estrogen-secreting pediatric ACTs highlighting their rare prevalence. This case stresses the need for a multidisciplinary approach to diagnosis, treatment, and long-term management of this entity in children and adolescents.

Indexed as

Adrenocortical adenomaAdrenocortical tumorCushing’s syndromeHypercortisolismHyperestrogenism

Identifiers

PMID42700419
PMCPMC13688359

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.