WordNet

a focal growth that resembles a neoplasm but results from faulty development in an organ

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腎臓の

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1. 腎血管筋脂肪腫 (AML)：マネージメントrenal angiomyolipomas amls management [show details]
…prognosis of renal AMLs. Other related issues are discussed elsewhere: Epidemiology, pathogenesis, clinical manifestations, and diagnosis of renal AMLs Renal manifestations of TSC Renal AMLs associated …
2. 腎血管筋脂肪腫 (AML)：疫学、病因、臨床症状および診断renal angiomyolipomas amls epidemiology pathogenesis clinical manifestations and diagnosis [show details]
…manifestations, and diagnosis of renal AMLs. Other related issues are discussed elsewhere: Management and prognosis of renal AMLs. Kidney manifestations of TSC. Renal AMLs associated with LAM. A general …
3. 腎の小腫瘤の診断法、鑑別診断、マネージメントdiagnostic approach differential diagnosis and management of a small renal mass [show details]
…are difficult to characterize on imaging and generally require further evaluation . When renal angiomyolipomas are bilateral, patients have an 80 to 90 percent chance of having tuberous sclerosis. Patients…
4. 結節性硬化症の腎症状renal manifestations of tuberous sclerosis complex [show details]
…prevalence of renal AMLs, the number and size of renal AMLs also increase with age . In the above series of children with TSC who had follow-up at a mean age of 10.5 years, growth of renal AMLs occurred in …
5. 孤発性リンパ脈管筋腫症：臨床症状と診断評価sporadic lymphangioleiomyomatosis clinical presentation and diagnostic evaluation [show details]
…chylous fluid). Renal AMLs – Renal AMLs occur in approximately one-third of women with sporadic LAM, which is much less frequent than in those with TSC-LAM (>80 percent) . Most renal AMLs can be readily …

English Journal

Wilms' tumor and benign renal tumor combined with hypospadias and incomplete orchiocatabasis appearing simultaneously in a 10 months old boy.

Li C, Li WS.
Urology journal. 2019 May;().
We herein report a case of left renal Wilms' tumor and right renal hamartoma combined with hypospadias and incomplete orchiocatabasis in a 10-month-old boy. In the literature to date, no case has been reported. The preoperative abdominal computerized tomography (CT) scan was suggestive of bilateral
PMID 31134609

[Tuberous Sclerosis Complex].

, K K, M M, M M, .
Brain and nerve = Shinkei kenkyu no shinpo. 2019 Apr;71(4)374-379.
Tuberous sclerosis complex (TSC) is an autosomal dominant inherited disorders that is characterized by the systemic hamartomas, along with epilepsy, cognitive impairment and hypopigmented macules. It is caused by genetic mutations in either TSC1 or TSC2 gene which encodes hamartin and tuberin, respe
PMID 30988224
PMID 30860727

Related Links

Renal Hamartoma (Angiomyolipoma) | Radiology

Renal hamartomas are considered benign tumors, probably arising from congenital rests within the organ. They contain various amounts of fat and smooth-muscle elements and are often rich in blood vessels. As a result of their “mixed” character, they have been variously designated as lipomata or angiolipomata (13), fibrolipomata, angiofibrolipoma, etc. (4, 8, 10, 11, 15, 16). While they have ...

Renal hamartoma: therapeutic aspects - PubMed

Hamartomas are benign renal tumors. In most cases they can be diagnosed by means of angiography. Treatment varies in accordance with clinical manifestation and progression. Symptom-free hamartomas need no treatment. In case of bleeding, embolization may be performed. Nephrectomy ought not to be performed save in emergency or if malignancy is ...

Renal Hamartoma - ScienceDirect

Renal Hamartoma. The Journal of Urology Vol. 66, No. 4, October 1951 Printed in U.S.A. RENAL HAMARTOMA CHARLES A. HÜLSE and EMIL E. PALIK From the Departments of Urology and Pathology at St. John's Hospital, Tulsa, Okla. Hamartoma has been defined by Albrecht as a tumor due to overdevelopment of some tissue element which belongs normally at ...