Items tagged “rare”

7 results found
Article

Primary prostatic malignant melanoma

Primary melanoma of the prostate is rare, and usually cannot be diagnosed on imaging alone. In many cases, it is believed that in fact, the tumor represents prostatic involvement by melanoma of the urethra. Epidemiology Primary malignant melanoma of the prostate represents both a tiny fraction...
Article

Primary urethral malignant melanoma

Melanoma of the urethra is a very rare tumor of the male urethra and often presents as an invasive prostatic mass. As such it is usually referred to as primary prostatic malignant melanoma.
Article

Prostate sarcoma

Prostate sarcomas are an uncommon and heterogeneous group of tumors arising from mesenchymal cells in and around the prostate (as opposed to the more common prostate adenocarcinoma which derives from the glandular tissue).  Pathology In children, the most common tumor type is a prostatic rhabd...
Article

Ossifying renal tumor of infancy

Ossifying renal tumor of infancy (ORTI) is a rare renal tumor. Epidemiology extremely rare, <<1% of pediatric renal neoplasms (17 cases reported) 6 days - 3 months male predominant Pathology Histology reveals spindle cells and osteoblastic cells in a calcified osteoid matrix. It is thought...
Article

Secretan disease

Secretan disease refers to rare situation of post-traumatic firm edema of the dorsum of the hand. The diagnosis can be considered in the setting of remote trauma and a fibrotic plaque-like lesion involving both the subcutaneous and tendinous spaces. Radiographic features MRI Signal characteri...
Article

12q14 microdeletion syndrome

12q14 microdeletion syndrome or osteopoikilosis-short stature-intellectual disability syndrome is caused by heterozygous deletion at the region of 12q14. The microdeletion affects the LEMD3 gene which has already been implicated in osteopoikilosis. Epidemiology Prevalence is <1 in 1 million li...
Article

Gardner-Silengo-Wachtel syndrome

Gardner-Silengo-Wachtel syndrome, also known as genito-palato-cardiac syndrome, is a rare male (46XY) gonadal dysgenesis condition that is assumed to be either an X-linked recessive or an autosomal recessive disorder 1. Epidemiology The estimated incidence is at <1 in 1,000,000 live births. P...