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  2. Cystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Cystic_kidney_disease

    Cystic kidney disease. Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions [1] and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life.

  3. Renal cyst - Wikipedia

    en.wikipedia.org/wiki/Renal_cyst

    Simple renal cyst. A renal cyst is a fluid collection in or on the kidney. There are several types based on the Bosniak classification. The majority are benign, simple cysts that can be monitored and not intervened upon. However, some are cancerous or are suspicious for cancer and are commonly removed in a surgical procedure called nephrectomy.

  4. Nephronophthisis - Wikipedia

    en.wikipedia.org/wiki/Nephronophthisis

    Infantile, juvenile, and adolescent forms of nephronophthisis have been identified. Although the range of characterizations is broad, people affected by nephronophthisis typically present with polyuria (production of a large volume of urine), polydipsia (excessive liquid intake), and after several months to years, end-stage kidney disease, a condition necessitating either dialysis or a kidney ...

  5. Adrenal insufficiency - Wikipedia

    en.wikipedia.org/wiki/Adrenal_insufficiency

    Adrenal insufficiency. Other names. adrenocortical insufficiency, hypocorticalism, hypocortisolism, hypoadrenocorticism, hypocorticism, hypoadrenalism. Adrenal gland. Specialty. Endocrinology. Adrenal insufficiency is a condition in which the adrenal glands do not produce adequate amounts of steroid hormones.

  6. Autosomal dominant polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    Medical genetics. Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, life-threatening inherited human disorders and the most common hereditary kidney disease. [1][2] It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and ...

  7. Polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Polycystic_kidney_disease

    Polycystic kidney disease. Polycystic kidney disease (PKD or PCKD, also known as polycystic kidney syndrome) is a genetic disorder [ 5 ][ 6 ] in which the renal tubules become structurally abnormal, resulting in the development and growth of multiple cysts within the kidney. [ 7 ] These cysts may begin to develop in utero, in infancy, in ...

  8. Acquired cystic kidney disease-associated renal cell carcinoma

    en.wikipedia.org/wiki/Acquired_cystic_kidney...

    Nephrology/oncology. Acquired cystic kidney disease-associated renal cell carcinoma is rare subtype of renal cell carcinoma. [1] It is most commonly seen in people with end-stage kidney disease who have a much higher risk of developing acquired cystic kidney disease (ACKD). Affected individuals have small kidneys with several cysts and their ...

  9. Adrenal haemorrhage - Wikipedia

    en.wikipedia.org/wiki/Adrenal_haemorrhage

    Adrenal haemorrhage. Adrenal hemorrhage (AH) is acute blood loss from a ruptured vessel of the adrenal glands above the kidneys. It is a rare, yet potentially fatal event that could be caused by trauma and multiple non-traumatic conditions. [1] Despite the unclear etiology, there are several risk factors of adrenal hemorrhage, including birth ...