Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Unicentric castleman disease in the differential diagnosis of a paravesical mass: A case report
1Department of Obstetrics and Gynaecology, Santa Casa de Misericórdia Hospital, Vitória, Espírito Santo, Brazil
2Department of Pathology, Santa Casa de Misericórdia Hospital, Vitória, Espírito Santo, Brazil
DOI: 10.31083/j.ejgo.2020.04.5268 Vol.41,Issue 4,August 2020 pp.644-647
Submitted: 24 May 2019 Accepted: 08 August 2019
Published: 15 August 2020
*Corresponding Author(s): Luyanne Azevedo Cabral Ferreira E-mail: lazcabral@gmail.com
Castleman disease is a rare condition with variable forms of clinical presentation. Diagnosis is therefore difficult and the ideal management of the disease has yet to be defined. Prognosis varies as a function of histologic type. Treatment can range from curative surgery for the unicentric form of the disease to a combination of treatments for the multicentric form. This paper describes an unusual case of unicentric Castleman disease in which the differential diagnosis included several gynaecological malignancies. The lesion was resected, with histopathology and immunohistochemistry confirming the diagnosis. The surgical procedure was completed without complications and follow-up of the patient over one year has shown no signs of recurrence. A literature review was performed, and the possible conditions to be included within the differential diagnoses are discussed.
Castleman disease; Unicentric Castleman disease; Paravesical mass; Pelvic tumors
Luyanne Azevedo Cabral Ferreira,Rafaela de Lacerda Trajano Pinel,Rodrigo Neves Ferreira,Antônio Chambô Filho. Unicentric castleman disease in the differential diagnosis of a paravesical mass: A case report. European Journal of Gynaecological Oncology. 2020. 41(4);644-647.
[1] Yamashita T., Mattos A.C., Ferreira M.C., Alvarenga M.: “Castleman’s disease: hyperplasia resembling a neoplasia”. Rev. Ciênc. Méd., 2006, 15, 173.
[2] Muhsein K.A., Liew N.C., Shaker A.R., Shahrin I.A.: “Localized Castleman’s disease presenting as a vascular right iliac fossa mass”. Asian J. Surg., 2004, 27, 54.
[3] Leitão S., Santos R., Jesus E., Santos A., Crespo J., Martins Y., et al.: “Castleman disease”. Medicina Interna. 1996, 3, 223.
[4] Oliveira C.V., Gonçalves C.E., Almeida V.F., Oliveira A.M., Pi- menta F.C.: “Abdominal Castleman’s disease”. Rev. Bras. Hematol. Hemoter., 2005, 27, 133.
[5] Szalat R., Munshi N.C.: “Diagnosis of Castleman disease”. Hematol Oncol Clin North Am.2018, 32, 53.
[6] Fajgenbaum D.C., Shilling D.: “Castleman disease pathogenesis”. Hematol. Oncol. Clin. North Am., 2018, 32, 11.
[7] Brito A.J., Salles C.E., Matiolla L.R., Reis T.G., Fava A.S.: “Relato de caso: doença de Castleman”. Rev. Bras. Cir. Cabeça Pescoço. 2009, 38, 120.
[8] Mendonça C., Rios E., Reis C., Santos A., Silva P.S.: “Castleman disease: clinical case report”. Medicina Interna, 2008, 15, 249.
[9] Simpson D.: “Epidemiology of Castleman disease”. Hematol. Oncol. Clin. North Am. 2018, 32, 1.
[10] Wagner N., Maden Z.:“An unusual unifocal presentation of Castleman’s disease in a young woman with a detailed description of sonographic findings to reduce diagnostic uncertainty: a case report”. BMC Res. Notes, 2013, 6, 97.
[11] Zhang Y., Zhai Y., Zhang Z.: “Castleman’s disease mimicked gynaecological adnexal tumour”. J. Obstet. Gynaecol., 2014, 34, 544.
[12] Wu D., Lim M.S., Jaffe E.S.: “Pathology of Castleman disease”. Hematol. Oncol.Clin. North Am. 2018, 32, 37.
[13] Chronowski G.M., Ha C.S., Wilder R.B., Cabanillas F., Manning J., Cox J.D.: “Treatment of unicentric and multicentric Castleman disease and the role of radiotherapy”. Cancer, 2001, 92, 670.
Top