Create issue ticket

447 Possible Causes for Lipoma, Neurofibromatosis Type 1

  • Legius Syndrome

    Additional clinical manifestations reported commonly include intertriginous freckling, lipomas, macrocephaly, and learning disabilities / ADHD / developmental delays.[] KEYWORDS: Legius syndrome; SPRED1; cafe-au-lait macules; neurofibroma; neurofibromatosis type 1[] Other less common manifestations include short stature, macrocephaly, Noonan-like facies, pectus excavatum/carinatum, lipomas, hypopigmented macules, vascular lesions, learning[]

  • Pheochromocytoma-Islet Cell Tumor Syndrome

    Furthermore, MEN type 1 may manifest in pituitary adenoma and non-endocrine tumors like angiofibroma, collagenoma, and lipoma.[] type 1 (NF1).[] type 1 (NF1), among others.[]

  • Proteus Syndrome

    A 7-year-old male is presented with a marked craniofacial deformation from a bony tumor containing an intraosseous lipoma.[] type 1 and other PHTS disorders (see these terms).[] The histopathological diagnosis of this mass was lipoma.[]

  • Familial Angiolipomatosis

    […] a lipoma.[] Abstract Familial angiolipomatosis is a rare syndrome that may be confused clinically with neurofibromatosis type 1.[] Familial angiolipomatosis may sometimes be clinically confused with neurofibromatosis type 1 (NF1), interestingly, Cina et al.[4] reported the occurrence of Lisch nodules[]

  • Hypertelorism

    In addition, she had previously undescribed manifestations including ventricular septal defect, lipoma of the occipital area, and hypoplastic left hemisphere of the cerebellum[] Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions V-F Mautner 1 , L Kluwe 1 , R E Friedrich 1 , A[] Associations with increased interorbital distance are also discussed: orofacial clefting, nonprotruding lipomas of the corpus callosum, calcification of the falx cerebri,[]

  • Neurofibromatosis Type 1

    How common is neurofibromatosis type 1? Neurofibromatosis type 1 occurs in 1 in 3,000 to 4,000 people worldwide. What genes are related to neurofibromatosis type 1?[] […] exophthalmos (5), li-fraumeni syndrome (5), malignant spindle cell melanoma (5), subclavian artery aneurysm (5), amyloid tumor (5), chronic polyneuropathy (4), pleomorphic lipoma[] […] neuroma Neurotized nevus Superficial angiomyxoma Nerve sheath myxoma Malignant peripheral nerve sheath tumor (MPNST) Dermatofibrosarcoma protuberans (DFSP) Spindle cell lipoma[]

  • Adiposis Dolorosa

    It is characterized by painful, irregular fatty swellings or lipomas and is frequently misdiagnosed.[] type 1 (NF1) and multiple endocrine neoplasia type 1 (see these terms).[] Abstract Adiposis dolorosa is a rare condition characterized by multiple painful lipomas.[]

  • Gardner Syndrome

    type 1.[] Facts : Autosomal dominant condition Colonic polyps with prominent extraintestinal lesions History / PE : Desmoid tumors Sebaceous or epidermoid cysts Lipomas Osteomas (especially[] Skin findings include epidermoid cyst, fibroid, lipoma, leiomyoma ve desmoid tumors.[]

  • Multiple Hamartoma Syndrome

    Further workup revealed additional smaller meningiomas, a parotid arteriovenous malformation, a lung cyst and pancreatic lipomas.[] Differential diagnosis Differential diagnoses, juvenile-polyposis syndrome, Peutz-Jeghers syndrome, Birt-Hogg-Dubé syndrome, Gorlin syndrome and neurofibromatosis type 1 ([] These syndromes include Neurofibromatosis type 1, tuberous sclerosis complex, Birt-Hogg-Dube, Peutz-Jeghers syndrome and Cowden syndrome [ 12 ].[]

  • Plexiform Neurofibroma

    A case of an isolated back plexiform neurofibroma, initially thought to be a lipoma, is presented, with emphasis on the importance of eliciting family history in reaching[] type 1.[] […] neuroma Neurotized nevus Superficial angiomyxoma Nerve sheath myxoma Malignant peripheral nerve sheath tumor (MPNST) Dermatofibrosarcoma protuberans (DFSP) Spindle cell lipoma[]

Further symptoms

Similar symptoms