Angiolipomas are benign subcutaneous tumors that usually present on the arms, legs, and trunk in young men. Angiolipomas typically range in size from 1 to 4 cm in diameter, and multiple lesions often are present. [mdedge.com]

Abstract Angiolipomas are among the most common benign soft-tissue tumors and usually present as solitary nodules; however, angiolipomas also may present as multiple subcutaneous nodules, typically on the arms and trunk of young men. [ncbi.nlm.nih.gov]

• Soft Tissue Swelling

  On inquiry, he had multiple painless soft-tissue swellings over his left forearm and abdomen, with a family history of similar swellings in his father and two brothers. [asianjns.org]

• Subcutaneous Mass

  The onset of these conditions occurred after the development of the subcutaneous masses by years to decades. The subcutaneous masses were not associated with antecedent medications or systemic infections. [escholarship.org]

  The autosomal dominant form of familial angiolipomatosis may be mistaken for peripheral neurofibromatosis (NF-1) due to the similarity of the family history and the occurrence of multiple subcutaneous masses, but histopathological examination of the tumors [ncbi.nlm.nih.gov]

  Abstract An 80-year-old man presented with a 50-year history of asymptomatic, subcutaneous masses on the arms, trunk, and legs. His father and maternal grandmother had had similar lesions. [wwww.unboundmedicine.com]

  There were multiple subcutaneous masses involving the chest wall and arms. Upon incarceration he stated that he had “neurofibromatosis”; there had been no clinical workup to support this diagnosis. [archivesofpathology.org]

• Papule

  Related Articles Dermpath Diagnosis Clear Cell Fibrous Papule Author: Ryan Yu, MD Samih Salama, MD, FRCPC Salem Alowami, MB Bch, FRCP A fibrous papule is a common benign lesion that usually presents in adults on the face, especially on the lower portion [mdedge.com]

  Similar lesions (piezogenic wrist papules) have been reported on the wrist. 42 A case of piezogenic palmar papules has been reported. 43 It was due to a subcutaneous lipoma that herniated into the dermis at several points. 43 Infantile pedal papules, [plasticsurgerykey.com]

  […] neurofibromatosis type 1, also familial angiolipomatosis, a benign condition with no malignant potential (Arch Pathol Lab Med 1999;123:946) Clinical images Images hosted on other servers: Lisch nodules Microscopic (histologic) description Dome shaped papules [pathologyoutlines.com]

• Pruritus

  Psoriasis/epidemiology, Adolescent, Adult, Aged, Aged, 80 and over, Algeria/epidemiology, Cross-Sectional Studies, Female, Humans, Incidence, Male, Middle Aged, Morocco/epidemiology, Pruritus/epidemiology, Pruritus/etiology, Psoriasis/etiology, Psoriasis [pesquisa.bvsalud.org]

• Suggestibility

  This condition is most often inherited in an autosomal recessive manner; however, several reports have been published suggesting an autosomal dominant mode of inheritance. [ncbi.nlm.nih.gov]

  However, he did not manifest any skin lesions suggestive of NF1. His son and grandson had similar subcutaneous tumors. [jstage.jst.go.jp]

• Babinski Sign

  Hyperreflexia was elicited in bilateral lower limbs with ill-sustained ankle clonus, bilateral Babinski's sign, and absent abdominal reflex. [asianjns.org]

• Clonus

  Hyperreflexia was elicited in bilateral lower limbs with ill-sustained ankle clonus, bilateral Babinski's sign, and absent abdominal reflex. [asianjns.org]

• Limb Weakness

  Case Report A 32-year-old man presented with a 20-day history of progressively severe imbalance on walking with bilateral lower limb weakness, gradually increasing numbness extending from the upper abdomen to both lower limbs, and dysesthesia on walking [asianjns.org]

• Dysesthesia

  The patient had immediate postoperative improvement of his weakness, dysesthesia, and urinary complaints and was mobilized on the 2nd postoperative day. [asianjns.org]

• Hyperreflexia

  Hyperreflexia was elicited in bilateral lower limbs with ill-sustained ankle clonus, bilateral Babinski's sign, and absent abdominal reflex. [asianjns.org]

Upon incarceration he stated that he had “neurofibromatosis”; there had been no clinical workup to support this diagnosis. [archivesofpathology.org]

• Hypertriglyceridemia

  家族性IV型高脂血症 familial hypertriglyceridemia 家族性高トリグリセリド血症 familial hypertriglyceridemia 家族性高中性脂肪血症 fasting 空腹時 fasting 絶食 fasting blood glucose 空腹時血糖 fasting blood glucose 空腹時血糖値 fasting blood glucose 空腹時全血ブドウ糖 fasting euglycemia 空腹時正常血糖 fasting hyperglycemia [jds.or.jp]

  However, the patient presented above had hypertriglyceridemia and low HDL cholesterol levels. Moreover, familial multiple lipomatosis might coexist with other diseases. [odermatol.com]

• Human Herpesvirus 8

  Kaposi sarcomas usually have slitlike vascular spaces, contain globules in the cytoplasm of some cells that are positive on periodic acid–Schiff staining, display immunoreactivity for human herpesvirus 8, and lack microthrombi. [mdedge.com]

• Lymph Node Hyperplasia

  PMID: 8249957 Giant lymph node hyperplasia in an angiolipomatous mediastinal mass. Madero S, Oñate JM, Garzón A. Arch Pathol Lab Med. 1986 Sep;110(9):853-5. PMID: 3755897 Angiofollicular lymphoid hyperplasia in an angiolipomatous mass. [humpath.com]

TY - JOUR T1 - Multiple familial angiolipomatosis: treatment of liposuction. [wwww.unboundmedicine.com]

Familial lipomatosis and angiolipomatosis do not require medical or surgical treatment. Liposuction [8] and surgical excision offer cosmetic and practical benefit to patients whose tumors are disfiguring or unusually large. [escholarship.org]

Ways To Give Home News Log In Appointments About Staff Collaborators Contact Us Treatments Research Dercum’s Disease Familial Multiple Lipomatosis (Angiolipomatosis) Lipedema Multiple Symmetric Lipomatosis SAT Disorders relationship to Obesity Resources [treat.medicine.arizona.edu]

[…] dominant inheritance in familial angiolipomatosis. 61 Kumar R...Chugh KS 2706802 1989 10 Autosomal dominant familial angiolipomatosis clinically mimicking neurofibromatosis. 61 Goodman JC...Baskin DS 2518515 1989 11 Multiple familial angiolipomatosis: treatment [malacards.org]

Liposuction has been used for the treatment of solitary lipomas, but to our knowledge liposuction has not previously been reported for excision of angiolipomas or in familial cases involving multiple lipomas as described here. [journals.lww.com]

(Outcomes/Resolutions) The prognosis of Adolescent Nephronophthisis is typically guarded. [dovemed.com]

So this means prognosis depends on the medical conditions present or co-morbidities. If there is, the prognosis is shorter. [medhelp.org]

Prognosis MSL is basically a benign condition but in some cases, there may be serious physical, cosmetic and psychological repercussions. Associated disorders may affect the prognosis. [orpha.net]

ERBB2 mutation is associated with a worse prognosis in patients with CDH1 altered invasive lobular cancer of the breast. [apps.medicine.uab.edu]

An 8–year‐old sister had similar tumors, suggesting a genetic etiology. The full text of this article hosted at iucr.org is unavailable due to technical difficulties. [onlinelibrary.wiley.com]

Carcinoma/radiotherapy, Laryngeal Neoplasms/radiotherapy, Pemphigus/etiology, Radiation Injuries/etiology, Acantholysis/drug therapy, Acantholysis/etiology, Acantholysis/pathology, Adrenal Cortex Hormones/therapeutic use, Antigens/immunology, Antineoplastic [pesquisa.bvsalud.org]

Etiology The pathogenesis of MSL is not fully understood, but it may be related to defective noradrenergic regulation of mitochondria in brown fat. The disease is strongly associated with alcohol abuse (up to 90% of patients). [orpha.net]

It could indicate that they do not segregate with FML phenotype, being discarded at least in this family as an etiological cause. [dovepress.com]

(Etiology) Adolescent Nephronophthisis is an inherited genetic disorder, and the inheritance pattern is autosomal recessive. [dovemed.com]

Psoriasis/epidemiology, Adolescent, Adult, Aged, Aged, 80 and over, Algeria/epidemiology, Cross-Sectional Studies, Female, Humans, Incidence, Male, Middle Aged, Morocco/epidemiology, Pruritus/epidemiology, Pruritus/etiology, Psoriasis/etiology, Psoriasis [pesquisa.bvsalud.org]

Images Angiolipoma: "angio" component; painful; intravasc thrombi Digital slides UI:738 - Subcutaneous angiolipoma (Lipohemangioma) Epidemiology Arises shortly before puberty or in young adults Rare in children or older adults 5% familial Localization [humpath.com]

Definition / general Subcutaneous nodule composed of mature adipocytes, thin walled vessels and fibrin thrombi Epidemiology Arises shortly before puberty or in young adults Rare in children or older adults 5% familial Clinical features Usually skin, 2 [pathologyoutlines.com]

Summary Epidemiology Multiple symmetric lipomatosis (MSL) primarily affects men and has a sex ratio of 15:1 to 30:1, depending on the region. The disorder may occur in all ethnic groups. [orpha.net]

Epidemiology It is generally seen in young adults or shortly after puberty. It is rarely seen in older adults and children. It has a 5% familial tendency of occurrence. [medmum.com]

Dercum's disease has a predilection to obese patients and this fact is mainly explained by the increased amount of fatty tissue, with the latter being an important key point in the disease pathophysiology. [academic.oup.com]

"Clinical and Pathophysiological Implications of a Bicuspid Aortic Valve" by P Fedak, et.al., Circulation 2002 2004 - A paper from Cincinnati Children's Hospital presents a study of the inheritance of BAVD. [bicuspidfoundation.com]

This case offers the opportunity to discuss the possible pathophysiological mechanisms underlying cluster-like headaches symptoms and the relation with pain referral from cervical structures to the head. [researchgate.net]

The pathophysiology of spinal vascular malformations. 1. Neurol. Sci. 23, (1974). Aminoff, M.J., Logue, V.: Clinical features of spinal vascular malformations. [docplayer.net]

Barrett's oesophagus: pathophysiology, diagnosis, and management. Scand J Gastroenterol 1998; 33: 449-453. 2. Romero Y, Cameron AJ, Locke GR 3rd, Schaid DJ, Slezak JM, Branch CD, Melton LJ. [hccpjournal.biomedcentral.com]

Awareness of the autosomal-dominant form of this entity is important to prevent its misdiagnosis as neurofibromatosis type I, which has a similar family history and clinical presentation. [mdedge.com]

Melanoma is the most deadly form of skin cancer and it is preventable/treatable. [davinciplastic.com]

Currently, there are no specific methods or guidelines to prevent the Adolescent Nephronophthisis, since it is a genetic condition Genetic testing of the expecting parents (and related family members) and prenatal diagnosis (molecular testing of the fetus [dovemed.com]