Condition | Indicated | Relationship Strength | Studies | Trials |
Cyst [description not available] | 0 | 1.94 | 1 | 0 |
Benign Neoplasms [description not available] | 0 | 1.94 | 1 | 0 |
Cancer of Pituitary [description not available] | 0 | 1.94 | 1 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 1.94 | 1 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 6.94 | 1 | 0 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 1.94 | 1 | 0 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 1.94 | 1 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 2.37 | 2 | 0 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 2.37 | 2 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 1.98 | 1 | 0 |
Cancer of Kidney [description not available] | 0 | 1.98 | 1 | 0 |
Kidney, Polycystic [description not available] | 0 | 1.98 | 1 | 0 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 1.98 | 1 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 1.98 | 1 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 1.98 | 1 | 0 |
Scrotal Hydrocele [description not available] | 0 | 1.97 | 1 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 1.97 | 1 | 0 |