Computerised Tomography Appearances of Partial Lipodystrophy Syndrome in Association with Membranoproliferative Glomerulonephritis Type 2
نویسنده
چکیده
Partial lipodystrophy is a disease in which body fat is lost in an unusual distribution, with patients often having a typically gaunt facial appearance. The disease is sometimes seen in association with mesangiocapillary glomerulonephritis type 2. We describe the computerised tomography features in such a patient and demonstrate the unusual fatty distribution that may occur. To our knowledge these findings have not been previously described in the international literature.
منابع مشابه
A possible association of partial lipodystrophy with anti-GBM nephritis (Goodpasture's syndrome).
Partial lipodystrophy is known to be associated with mesangiocapillary glomerulonephritis. A case is described of a possible association of partial lipodystrophy with anti-GBM nephritis (Goodpasture's syndrome).
متن کاملThe pregnant patient with partial lipodystrophy developing acute renal failure--onset of de novo membranoproliferative glomerulonephritis.
The pregnant patient with partial lipodystrophy developing acute renal failure—onset of de novo membranoproliferative glomerulonephritis Key words: acute renal failure; pregnancy; partial lipo-towards the end of the gestation period, between 34 dystrophy; low C3; membranoproliferative nephritis and 38 weeks, and it is invariably the result of pre-eclampsia and its complications or the result of...
متن کاملType III Mixed Cryoglobulinemia and Antiphospholipid Syndrome in a Patient With Partial DiGeorge Syndrome
We studied a 14 year-old boy with partial DiGeorge syndrome (DGS), status post complete repair of Tetralogy of Fallot, who developed antiphospholipid syndrome (APS) and type III mixed cryoglobulinemia. He presented with recurrent fever and dyspnea upon exertion secondary to right pulmonary embolus on chest computed tomography (CT). Coagulation studies revealed homozygous methylene tetrahydrofol...
متن کاملThe patient with glomerulonephritis and lipodystrophy.
In 1979, heavy proteinuria and microscopic haematuria lytic anaemia, with a positive Coombs’ test using an anticomplement reactant. Other immunological feawere discovered in a 25-year-old man following an upper respiratory tract infection. He was hospitalized tures consisted of decreased levels of C3, normal levels of C4, and presence of C3 NeF (nephritic factor), in a nephrology unit. Physical...
متن کاملCrescentic C3 glomerulopathy with acquired partial lipodystrophy: An unusual cause of rapidly progressive renal failure.
Complement component C3 glomerulopathy (C3GP) is a recently defined entity characterized by predominant glomerular C3 fragment deposition with absent or scanty immunoglobulin deposition due to abnormal control of complement activation, deposition, or degradation.[1] C3GP is subcategorized morphologically into dense deposit disease (DDD) and C3 glomerulonephritis (C3GN) based on electron microsc...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2001