| NF | Neuro-Fibromatosis = Von Recklinghausen's Disease NF 1; Neuro-Fibroma... |
|---|---|
| RF | radial fiber; radio frequency; receptive field; regurgitant fraction; Reitland-Franklin [unit]; rela... |
| GFD | gingival fibromatosis-progressive deafness [syndrome]; gluten-free diet |
| IRF | idiopathic retroperitoneal fibrosis; impulse response function; interferon regulatory factor; intern... |
| RP | radial pulse; radiopharmaceutical; rapid processing [of film]; Raynaud phenomenon; reactive protein;... |
| RF | retroperitoneal fibromatosis |
|---|---|
| JHF | Juvenile Hyalin Fibromatosis |
| IRF | Idiopathic Retroperitoneal Fibrosis |
| RP | Retroperitoneal |
| RPF | Retroperitoneal fibrosis |
| retroperitoneal | <anatomy> Behind or posterior to the peritoneum. (11 Jan 1998) |
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| retroperitoneal adenopathy | <radiology> Ultrasound: increased echo most likely to be adenocarcinoma, decreased echo most likely to be lymphoma (12 Dec 1998) |
| retroperitoneal fibrosis | <radiology> Ureters tapered or obstructed, most severe at L4-5, ureters deviated medially, Treatment: symptomatic; steroids have ? long-term benefit Differential diagnosis: malignancy, lymphoma (especially Hodgkin's), metastasis from colon and breast, retroperitoneal sarcoma, drugs, methysergide (Sansert), haemorrhage, aortic aneurysm, trauma or surgery, inflammation, Crohn's disease, diverticulitis, pancreatitis, extravasated urine, radiation (12 Dec 1998) |
| retroperitoneal hernia | A hernia in the subperitoneal tissues. Synonym: retroperitoneal hernia, Treitz's hernia. (05 Mar 2000) |
| retroperitoneal liposarcoma | <radiology> Most common primary retroperitoneal tumour, rarely arises from lipoma, 95% of all fatty retroperitoneal tumours, 40-60 years; M>F, most radiosensitive sarcoma (32% 5-year survival) findings, CT, contrast enhancement, mixed density (fat and soft tissue elements), pseudocystic pattern: water density secondary to volume averaging, angio: hypovascular; no vessel dilation, capillary staining, laking sites for liposarcoma: lower extremity 45%, abdominal cavity and retroperitoneum 14%, trunk 14%, upper extremity 8%, head and neck 7% (12 Dec 1998) |
| retroperitoneal space | An area occupying the most posterior aspect of the abdominal cavity. It is bounded laterally by the borders of the quadratus lumborum muscles and extends from the diaphragm to the brim of the true pelvis, where it continues as the pelvic extraperitoneal space. (12 Dec 1998) |
| abdominal fibromatosis | <anatomy> Resembling, or having the characteristics of, a ligament; ligamentous. Origin: Gr. Desmos ligament. Source: Websters Dictionary (01 Mar 1998) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| palmar fibromatosis | Nodular fibroplastic proliferation in the palmar fascia of one or both hands, preceding or associated with Dupuytren's contracture. (05 Mar 2000) |
| gingival fibromatosis | Fibromatosis that may be associated with trichodiscomas. Several genetic forms are known, all autosomal dominant . (05 Mar 2000) |
| penile fibromatosis | A disease of unknown cause in which there are plaques or strands of dense fibrous tissue surrounding the corpus cavernosum of the penis, causing deformity and painful erection; sometimes associated with Dupuytren's contracture. Synonym: penile fibromatosis, van Buren's disease. (05 Mar 2000) |
| plantar fibromatosis | Nodular fibroblastic proliferation in plantar fascia of one or both feet; rarely associated with contracture. Synonym: Dupuytren's disease of the foot. (05 Mar 2000) |
| congenital generalised fibromatosis | Multiple subcutaneous and visceral fibrous tumours present at birth; a rare disorder often fatal in the first week of life, although sometimes undergoing spontaneous remission; probable autosomal recessive inheritance. (05 Mar 2000) |
| infantile digital fibromatosis | Multiple fibrous flesh-coloured nodules on the extensor aspect of the terminal phalanges of adjacent digits of infants and young children which often recur after attempted excision, do not metastasize, and may spontaneously regress in two to three years; composed of spindle cells containing cytoplasmic inclusions believed to be derived from myofibrils. Synonym: infantile digital fibromatosis. (05 Mar 2000) |
| juvenile hyalin fibromatosis | A rare recessively inherited deforming disorder of head, neck, and generalised cutaneous nodules or tumours in children with normal mentality; the lesions consist of fibroblasts separated by an eosinophilic hyalin stroma composed mostly of glycosaminoglycans. Synonym: systemic hyalinosis. (05 Mar 2000) |
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