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  • fibrous histiocytoma
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  • histiocytoma
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  • lipoid
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  • lipoid cell
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  • lipoid
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  • eruptive histiocytoma
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  • fibrous histiocytoma
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  • generalized eruptive histiocytoma
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  • giant cell histiocytoma
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  • histiocytoma
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  • lipoidal histiocytoma
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  • malignant fibrous histiocytoma
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  • histiocytoma,fibrous
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  • epithelioid histiocytoma
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  • eruptive histiocytoma
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  • fibrous histiocytoma
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  • fibrous histiocytoma,malignant
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  • histiocytoma
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  • familial lipoid degeneration
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CGFH congenital fibrous histiocytoma
CLAH congenital lipoid adrenal hyperplasia
LN Lesch-Nyhan [syndrome]; lipoid nephrosis; Lisch nodule; low necrosis; lupus nephritis; lymph node
MFH malignant fibrous histiocytoma
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lipoid CAH lipoid adrenal hyperplasia
LN lipoid nephrosis
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  • fibrous histiocytoma
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  • histiocytoma cutis
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malignant fibrous histiocytoma <tumour> A deeply situated tumour, especially on the extremities of adults, frequently recurring after surgery and metastasizing to the lungs; shows partial fibroblastic and histiocytic differentiation with a variable storiform pattern, myxoid areas, and giant cells.
(05 Mar 2000)
generalised eruptive histiocytoma A rare recurring generalised eruption in adults of flesh coloured or erythematous papules remaining localised to the skin and consisting of dermal nodules of mononuclear histiocytes that do not stain for lipid.
Synonym: nodular non-X histiocytosis.
(05 Mar 2000)
histiocytoma <tumour> A tumour composed of histiocytes.
Origin: histio-+ G. Kytos, cell, + -oma, tumour
(05 Mar 2000)
histiocytoma, fibrous A tumour composed, wholly or in part, of cells with the morphologic characteristics of histiocytes and with various fibroblastic components. There are many variants and many names. Superficially located histiocytic lesions behave benignly but deep, benign histiocytomas may invade locally into surrounding tissue. Fibrous histiocytomas can occur anywhere in the body. Superficial lesions are always cured by simple excision; a wider margin of tissue should be obtained for deep, benign types. Local recurrence is uncommon.
(12 Dec 1998)
hypothalamic histiocytoma <radiology> Parasellar tumour, may not be able to differentiate from: suprasellar (optic nerve/chiasm) glioma, teratoma, kids with tumour usually have, diabetes insipidus, skeletal lesions of histiocytosis
(12 Dec 1998)
nephrosis, lipoid Glomerular disease causing heavy proteinuria characterised by absence of obvious histologic glomerular changes on light microscopy. It is also called minimal change glomerular disease and minimal lesion glomerulonephritis.
(12 Dec 1998)
fibrous histiocytoma <tumour> A benign lung or bronchial lesion, often subpleural, sometimes multiple, which forms hyalinised connective tissue.
Synonym: fibrous histiocytoma.
(05 Mar 2000)
lipoid 1. Resembling fat.
2. Former term for lipid.
Synonym: adipoid.
Origin: Lipo-+ G. Eidos, appearance
(05 Mar 2000)
lipoid granuloma Granuloma characterised by aggregates or accumulations of fairly large mononuclear phagocytes that contain lipid.
(05 Mar 2000)
lipoid nephrosis <nephrology> A disorder of the kidneys which largely affects the glomerulus, the blood filtering structure. This disorder is one common cause of nephrotic syndrome in children affecting 2 to 3 children per 100,000 population under age 16 in the us. Minimal change disease is also seen rarely in adults.
The cause is unknown but may be related to an autoimmune illness. Risk factors include a history for a immune disorder, recent immunisation or a bee sting.
Diagnosis is made by renal biopsy. Treatment include systemic corticosteroids which are usually quite effective in curing this disease. Other medications include chlorambucil and cyclophosphamide. In most cases, a moderate protein diet (1 gram protein per Kg body weight per day) will be recommended. Salt (sodium) restriction can be helpful to reduce swelling and vitamin D is usually supplemented.
(27 Sep 1997)
lipoid proteinosis <disease> A familial disease occurring in the course of latent diabetes, marked by yellowish nodules due to deposits of a protein-lipid complex on the oral tongue and sublingual and faucial areas, translucent keratotic papillomatous eyelid lesions, keratotic lesions on the extremities, and hoarseness.
It is due to a disturbance of lipid metabolism with autosomal recessive inheritance and is frequently associated with intracranial calcifications.
inheritance: autosomal recessive.
Synonym: hyalinasis cutis et mucosae, lipoidosis cutis et mucosae, Urbach-Wiethe disease.
(05 Mar 2000)
lipoid theory of narcosis That narcotic efficiency parallels the coefficient of partition between oil and water, and that lipoids in the cell and on the cell membrane absorb the drug because of this affinity.
Synonym: Meyer-Overton theory of narcosis.
(05 Mar 2000)
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