ArticleCancer control : journal of the Moffitt Cancer Center2017
Primary Adrenal Angiosarcoma: A Rare and Potentially Misdiagnosed Tumor.
Article in Cancer control : journal of the Moffitt Cancer Center, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 16 citations in OpenAlex.
- Primary adrenal epithelioid angiosarcoma: An extraordinarily rare malignancy with a challenging diagnosis.Radiology case reports · 2026Article
- Adrenal angiosarcoma, a rare neoplasm: a case report and a literature review.Gland surgery · 2026Article
- Primary adrenal angiosarcoma: a rare case presentation.Journal of surgical case reports · 2025Article
- Spotlight on the Unusual: A Case Report of Adrenal Angiosarcoma Presenting as an Abdominal Mass.Cureus · 2025Article
- Article
- Epithelioid angiosarcoma of the adrenal gland with metastasis: a case report and literature review.Annals of medicine and surgery (2012) · 2023Article
- Incidental adrenal hemangioma clinically suspicious for malignancy: diagnostic considerations and review of the literature.International journal of clinical and experimental pathology · 2022Article
- Adrenal hemorrhage and hemorrhagic masses; diagnostic workup and imaging findings.The British journal of radiology · 2021Review
- Case Report: Postoperative Recurrence of Adrenal Epithelioid Angiosarcoma Achieved Complete Response by Combination Chemotherapy With Liposomal Doxorubicin and Paclitaxel.Frontiers in oncology · 2021Article
- Adrenal angiosarcoma with metastasis: Imaging and histopathology of a rare adrenal cancer.Radiology case reports · 2020Article
- Adrenal Angiosarcoma: A Diagnostic Dilemma.Cureus · 2019Article
- A case of angiosarcomas which occurred in an adrenal gland and spleen synchronously.International cancer conference journal · 2018Article
- A case report of primary adrenal angiosarcoma as depicted on magnetic resonance imaging.Medicine · 2017Article
Corrections and comments
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Authors and funding
9 authors at 1 institution in 1 country.
Funding
Abstract
A man aged 69 years presented with acute right flank pain secondary to a hemorrhagic large adrenal tumor. En bloc resection was performed to repair the inferior vena cava. Immunoperoxidase levels in the tumor were positive for factor VIII and CD31 and negative for S100, protein Melan-A, CD34, synaptophysin, chromogranin, desmin, muscle specific actin, ETFA (EMA), KRT20 (CK20), CDX2, TTF1, LNPEP (PLAP), inhibin, ?-fetoprotein, CD30, hepatocyte paraffin, and aberrant expression of cytokeratin 7 and pankeratin. The pathological diagnosis was consistent with adrenal angiosarcoma. Obtaining appropriate immunoperoxidase stains and multidisciplinary evaluation helped make the diagnosis of this rare adrenal tumor and determine its management. The patient had an uneventful postoperative course and completed 4 cycles of adjuvant chemotherapy with doxorubicin/ifosfamide and adequately tolerated the treatment. However, positive surgical margins were found, so he was referred to radiation oncology specialists for possible adjuvant radiotherapy to the surgical bed. Weeks after the first initiation of therapy, the patient presented to the emergency department complaining of shortness of breath, fatigue, and generalized weakness for 3 days. He was admitted and found to have new-onset anemia and a new-onset, large, right pleural effusion. Thoracentesis performed showed sanguinolent fluid that, after microscopic evaluation, was suggestive of recurrent malignancy. Thoracic aortography performed with subselective catheterization to several arteries (right bronchial, right phrenic, and right renal arteries) did not show any active bleeding. However, the right inferior intercostal and adrenal arteries were presumed to be the reason for the bleeding event, so they were embolized until stasis. The patient remained hemodynamically unstable but eventually experienced multiorgan failure. In spite of aggressive measures, he died 10 days after admission to the hospital.
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