clinical manifestation of retroperitoneal tuberculosis as pseudotumor in an 18-year-old female

Retroperitoneal Anaplastic Neuroblastoma in a 3-Year-Old Female: A Rare Case Report

Neuroblastoma is the most common extracranial solid tumor in childhood. In different classification of neuroblastomas, a subset of undifferentiated or poorly differentiated tumors with bizarre histological features has been mentioned. A 3-year-old girl presented with abdominal pain. Her haematological and biochemical parameters were normal except her urinary vanelylmandelic acid level was elevat...

An 18-year-old female with weight loss and hypokalemia.

Primary Splenic Tuberculosis in a 43-Year-Old Female Patient in Fatemi Hospital of Ardebil: A Case Report

Background and Objectives: Tuberculosis (TB) is included within the top ten causes of death worldwide. This disease is associated with pulmonary and extrapulmonary involvement. The major extra pulmonary organs involved in the disease, are lymph nodes, pleura, genitourinary tract, bones, and meningeal tissue. Primary splenic infection is one of the rare complications of TB.   Case Report: Patie...

Clear cell adenocarcinoma of the uterine cervix in an 18 year-old pregnant female☆

•An 18 year old nulliparous woman was diagnosed with clear cell adenocarcinoma of the cervix in pregnancy.•LEEP conization at 33.3 weeks gestation led to premature rupture of membranes. Following cesarean section, a radical hysterectomy was performed.

Cerebral infarction due to moyamoya disease in an 18 year old female.

Moyamoya disease was diagnosed as the cause of cerebral infarction in an 18 year old white female. The clinical features, pathology and treatment of this occlusive cerebrovascular disorder are discussed.

Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female.

The clinical features and cytogenetic results of an 18 year old mentally handicapped female found to be a mosaic for a tandem duplication of chromosome 1 (46,XX,dup(1)(q12q22)/46,XX) are reported. The case is compared with the three previously described cases and possible mechanisms for the origin of the duplication are discussed. This patient was not found to have features of Proteus syndrome ...