asymptomatic isolated retroperitoneal castleman’s disease: a case report

Authors

afsaneh rajabiani assistant professor of pathology, shariati hospital, tehran university medical of sciences

alireza abdollahi associate professor of pathology, imam khomeini hospital complex, vali-asr hospital, central laboratory, tehran university medical of sciences.

zahra farahani physiologist-research. maternal , fetal and neonatal research center, tehran university medical of sciences.

abstract

castleman’s disease, giant lymph node hyperplasia, is a kind of benign lymphoproliferative disease with gentle behavior. its etiology and prevalence are unclear. this rare disease is usually found in mediastinal area asymptomatically and incidentally. it is also rare to see this tumor in the retroperitoneum. in this study, we have introduced a 34-year-old woman who referred just with occasional abdominal pain caused by compressive symptoms. laboratory findings only reported microcytic anemia (mch: 18.5, mcv: 63, hemoglobin 10.2 g/dl). chest and abdominal x-ray imaging showed no remarkable point. in abdominal ultrasonography, a solid and firm tumor with 12.2×5.3×6.6 cm was reported in patient’s retroperitoneum. patient’s surgery was done and the tumor (covered by a fibrous thick capsule, with no bizarre appearance and bleeding) was completely removed. pathologic examination indicated a castleman’s tumor, type of unicentric and hyaline-vascular. this item had been one of the rare reported items of castleman’s disease in the retroperitoneal space.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Asymptomatic Isolated Retroperitoneal Castleman’s Disease: A Case Report

Castleman’s disease, giant lymph node hyperplasia, is a kind of benign lymphoproliferative disease with gentle behavior. Its etiology and prevalence are unclear. This rare disease is usually found in mediastinal area asymptomatically and incidentally. It is also rare to see this tumor in the retroperitoneum. In this study, we have introduced a 34-year-old woman who referred just with occasional...

full text

Asymptomatic Isolated Retroperitoneal Castleman’s Disease: A Case Report

Castleman's disease, giant lymph node hyperplasia, is a kind of benign lymphoproliferative disease with gentle behavior. Its etiology and prevalence are unclear. This rare disease is usually found in mediastinal area asymptomatically and incidentally. It is also rare to see this tumor in the retroperitoneum. In this study, we have introduced a 34-year-old woman who referred just with occasional...

full text

Isolated cutaneous Crohn’s disease: A case report

This case report describes a patient with cutaneous signs in the genital and peri-anal region suspicious of Crohn’s disease without any intestinal symptom or sign. Inflammatory bowel disease can be associated with some cutaneous signs. However, in this paper, we report a patient with isolated cutaneous Crohn’s disease which is very rare (less than 100 case reports across the world). Our patient...

full text

Retroperitoneal bronchogenic cyst: a case report

  Bronchogenic cysts are among developmental disorders of the primitive foregut which are typically found above the diaphragm. Bronchial cysts discovered in the abdominal cavity or retroperitoneum are extremely rare. We present a rare case of a retroperitoneal bronchogenic cyst which was incidentally detected after a wrestling injury in a 23-year-old man who had a negative medical history. Alth...

full text

Retroperitoneal Castleman disease: report of a case and review of the literature

 Abstract Castleman disease or giant node hyperplasia is a rare disorder of the lymphoid tissue most often involving the mediastinal lymph nodes. We report a case of localized retroperitoneal hyaline-vascular type of Castleman disease. A 35-year old woman presented with mild epigastric pain with radiation to the back. Amild anemia was the only abnormal associated finding. Abdominal ultrasound a...

full text

Isolated levocardia: A case report

Introduction: Levocardia with situs inversus, a rare congenital disorder, is usually associated with severe cyanotic congenital heart disease. Thus these patients have adverse prognosis. Case Report: A 2-day-old neonate with mild central cyanosis was admitted to Neonatal Intensive Care Unit (NICU). Prenatal sonographies were normal. Physical exam was normal except for 2/6 heart murmur in left s...

full text

My Resources

Save resource for easier access later


Journal title:
iranian journal of medical sciences

جلد ۴۰، شماره ۵، صفحات ۴۶۹-۰

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023