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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.[rasopathiesnet.org] KEYWORDS: Legius syndrome; SPRED1; cafe-au-lait macules; neurofibroma; neurofibromatosis type 1[ncbi.nlm.nih.gov] Other less common manifestations include short stature, macrocephaly, Noonan-like facies, pectus excavatum/carinatum, lipomas, hypopigmented macules, vascular lesions, learning[orpha.net]

  • Pheochromocytoma-Islet Cell Tumor Syndrome

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

  • Proteus Syndrome

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

  • Familial Angiolipomatosis

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

  • Hypertelorism

    In addition, she had previously undescribed manifestations including ventricular septal defect, lipoma of the occipital area, and hypoplastic left hemisphere of the cerebellum[ncbi.nlm.nih.gov] 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[doi.org] Associations with increased interorbital distance are also discussed: orofacial clefting, nonprotruding lipomas of the corpus callosum, calcification of the falx cerebri,[ncbi.nlm.nih.gov]

  • 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?[web.archive.org] […] exophthalmos (5), li-fraumeni syndrome (5), malignant spindle cell melanoma (5), subclavian artery aneurysm (5), amyloid tumor (5), chronic polyneuropathy (4), pleomorphic lipoma[genome.ucsc.edu] […] neuroma Neurotized nevus Superficial angiomyxoma Nerve sheath myxoma Malignant peripheral nerve sheath tumor (MPNST) Dermatofibrosarcoma protuberans (DFSP) Spindle cell lipoma[surgpathcriteria.stanford.edu]

  • Adiposis Dolorosa

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

  • Gardner Syndrome

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

  • Multiple Hamartoma Syndrome

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

  • 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[ncbi.nlm.nih.gov] type 1.[ncbi.nlm.nih.gov] […] neuroma Neurotized nevus Superficial angiomyxoma Nerve sheath myxoma Malignant peripheral nerve sheath tumor (MPNST) Dermatofibrosarcoma protuberans (DFSP) Spindle cell lipoma[surgpathcriteria.stanford.edu]

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