Literature DB >> 28441375

Primary Adrenal Angiosarcoma: A Rare and Potentially Misdiagnosed Tumor.

Ariel Grajales-Cruz, Francis Baco-Viera, Ernesto Rive-Mora, Carlos Ramirez-Tanchez, David Tasso, Norma Arroyo-Portela, Elizabeth Calderon, Ilean Joan Padua-Octaviani, William Caceres-Perkins1.   

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.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28441375      PMCID: PMC5483322          DOI: 10.1177/107327481702400213

Source DB:  PubMed          Journal:  Cancer Control        ISSN: 1073-2748            Impact factor:   3.302


  13 in total

Review 1.  Clinical practice. The incidentally discovered adrenal mass.

Authors:  William F Young
Journal:  N Engl J Med       Date:  2007-02-08       Impact factor: 91.245

2.  Angiosarcoma arising within a long-standing cystic lesion of the adrenal gland: a case report.

Authors:  Ji-Youn Sung; Soomin Ahn; Sung Joo Kim; Young Soo Park; Yoon-La Choi
Journal:  J Clin Oncol       Date:  2013-01-28       Impact factor: 44.544

Review 3.  Epithelioid angiosarcoma arising in an adrenal cortical adenoma: a case report and review of the literature.

Authors:  Shona Hendry; Cynthia Forrest
Journal:  Int J Surg Pathol       Date:  2014-04-25       Impact factor: 1.271

Review 4.  Adrenal angiosarcoma: report of a case.

Authors:  Enricomaria Pasqual; Franco Bertolissi; Franco Grimaldi; Carlo Alberto Beltrami; Cathrine Anne Scott; Stefano Bacchetti; Beata Ursula Waclaw; Pier Paolo Cagol
Journal:  Surg Today       Date:  2002       Impact factor: 2.549

5.  Epithelioid angiosarcoma of the adrenal glands. A clinicopathologic study of nine cases with a discussion of the implications of finding "epithelial-specific" markers.

Authors:  B M Wenig; S L Abbondanzo; C S Heffess
Journal:  Am J Surg Pathol       Date:  1994-01       Impact factor: 6.394

6.  Angiosarcoma of the adrenal gland.

Authors:  L R Kareti; S Katlein; S Siew; A Blauvelt
Journal:  Arch Pathol Lab Med       Date:  1988-11       Impact factor: 5.534

7.  Limited value of adrenal biopsy in the evaluation of adrenal neoplasm: a decade of experience.

Authors:  Peter J Mazzaglia; Jack M Monchik
Journal:  Arch Surg       Date:  2009-05

Review 8.  NIH state-of-the-science statement on management of the clinically inapparent adrenal mass ("incidentaloma").

Authors: 
Journal:  NIH Consens State Sci Statements       Date:  2002 Feb 4-6

Review 9.  Adrenal tumors with unexpected outcome: a review of the literature.

Authors:  Thomas M Kerkhofs; Rudi M Roumen; Thomas B Demeyere; Antoine N van der Linden; Harm R Haak
Journal:  Int J Endocrinol       Date:  2015-03-25       Impact factor: 3.257

Review 10.  A vinyl chloride-exposed worker with an adrenal gland angiosarcoma: a case report.

Authors:  Mario Criscuolo; Jacqueline Valerio; Maria Elena Gianicolo; Emilio A L Gianicolo; Maurizio Portaluri
Journal:  Ind Health       Date:  2013-12-02       Impact factor: 2.179

View more
  3 in total

1.  Adrenal Angiosarcoma: A Diagnostic Dilemma.

Authors:  Nirav Antao; Michael Ogawa; Zarir Ahmed; Jinhua Piao; Nishant Poddar
Journal:  Cureus       Date:  2019-08-12

2.  A case report of primary adrenal angiosarcoma as depicted on magnetic resonance imaging.

Authors:  Xue-Ming Li; Hong Yang; Jing Reng; Peng Zhou; Zhu-Zhong Cheng; Zhen Li; Guo-Hui Xu
Journal:  Medicine (Baltimore)       Date:  2017-11       Impact factor: 1.817

3.  Case Report: Postoperative Recurrence of Adrenal Epithelioid Angiosarcoma Achieved Complete Response by Combination Chemotherapy With Liposomal Doxorubicin and Paclitaxel.

Authors:  Hangping Wei; Jie Mao; Yandan Wu; Qinfei Zhou
Journal:  Front Oncol       Date:  2021-12-16       Impact factor: 6.244

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.