Mentioned in ?
References in periodicals archive ?
Spinal lipomas have been broadly classified into five clinical entities lipomyelomeningocele, fatty filum, intradural spinal mass, epidural lipomatosis, and spinal angiolipoma.
5%) by participants as compared to the lipomyelomeningocele form (12.
Although the classic example is the child with a myelomeningocele, a significant number of our patients have other spinal cord defects, including lipomyelomeningocele, fatty filum, and occult tethered cords.
PELVIS###Perineal hemangioma, external genitalia malformations, lipomyelomeningocele, vesicorenal abnormalities, imperforate anus, and skin tag.
Lipomyelomeningocele consists of a skin covered back mass that contains neural tissues, CSF, meninges and presence of lipoma or lipomatous component that extends from the subcutaneous tissue of back through the back mass into the spinal canal.
This can be caused by a variety of etiologies: myelomeningocele, lipomyelomeningocele, diastematomyelia, tight filum terminale, dermal sinus tract, tumor, and scar tissue.
We present the case of a 66-year-old woman born with a terminal lipomyelomeningocele, presenting with new fecal incontinence and a desire to undivert her ileal conduit.
org 1,3 LIMB-GIRDLE MUSCULAR DYSTROPHY See: Muscular Dystrophy LIMIT DEXTRINOSIS See: Glycogen Storage Diseases; Muscular Dystrophy LIPID HISTIOCYTOSIS See: Niemann-Pick Disease LIPIDOSIS, CEREBROSIDE See: Gaucher Disease LIPOFUSCINOSES, NEURONAL CEROID See: Batten Disease LIPOID HYPERPLASIA, CONGENITAL See: Adrenal Disorders LIPOMYELOMENINGOCELE Lipomyelomeningocele Family Support Network 321 Hopewell St.
org 1 LIMB-GIRDLE MUSCULAR DYSTROPHY See: Muscular Dystrophy LIMIT DEXTRINOSIS See: Glycogen Storage Diseases; Muscular Dystrophy LIPID HISTIOCYTOSIS See: Niemann-Pick Disease, LIPIDOSIS, CEREBROSIDE See: Gaucher Disease LIPOFUSCINOSES, NEURONAL CEROID See: Batten Disease LIPOID HYPERPLASIA, CONGENITAL See: Adrenal Disorders LIPOMYELOMENINGOCELE Lipomyelomeningocele Family Support Network 321 Hopewell St.
org 1,3 LIMB-GIRDLE MUSCULAR DYSTROPHY See: Muscular Dystrophy LIMIT DEXTRINOSIS See: Glycogen Storage Diseases; Muscular Dystrophy LIPID HISTIOCYTOSIS See: Niemann-Pick, Type C Disease LIPIDOSIS, CEREBROSIDE See: Gaucher Disease LIPOFUSCINOSES, NEURONAL CEROID See: Batten Disease LIPOID HYPERPLASIA, CONGENITAL See: Adrenal Disorders LIPOMYELOMENINGOCELE Lipomyelomeningocele Family Support Network 321 Hopewell St.
Newton, MA 02460-2250 1,3 LIMB-GIRDLE MUSCULAR DYSTROPHY See: Muscular Dystrophy LIMIT DEXTRINOSIS See: Glycogen Storage Diseases; Muscular Dystrophy LIPID HISTIOCYTOSIS See: Niemann-Pick Disease LIPIDOSIS, CEREBROSIDE See: Gaucher Disease LIPOFUSCINOSES, NEURONAL CEROID See: Batten Disease LIPOMYELOMENINGOCELE Lipomyelomeningocele Family Support Network 321 Hopewell St.