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The New England Journal of Medicine, ISSN 0028-4793, 01/2008, Volume 358, Issue 2, pp. 140 - 151
Journal Article
Journal Article
Surgical Pathology Clinics, ISSN 1875-9181, 06/2016, Volume 9, Issue 2, pp. 269 - 287
This review covers gynecologic manifestations that may occur in rare hereditary syndromes. Recent advances in disorders, such as hereditary leiomyomatosis,... 
Cowden syndrome | Maffucci syndrome | Hereditary leiomyomatosis renal cell carcinoma syndrome | Tuberous sclerosis | Von Hippel-Lindau | Ollier disease | Carney complex | Nevoid basal cell carcinoma syndrome | Neoplastic Syndromes, Hereditary - pathology | Prognosis | Uterine Neoplasms - pathology | Humans | Lymphangioleiomyomatosis - pathology | Carney Complex - pathology | von Hippel-Lindau Disease - diagnosis | Genital Neoplasms, Female - diagnosis | Tuberous Sclerosis - pathology | Basal Cell Nevus Syndrome - pathology | von Hippel-Lindau Disease - pathology | Leiomyomatosis - diagnosis | Skin Neoplasms - diagnosis | Carney Complex - genetics | Leiomyomatosis - pathology | Female | Neoplastic Syndromes, Hereditary - genetics | Tuberous Sclerosis - diagnosis | Uterine Neoplasms - diagnosis | Carney Complex - diagnosis | Genital Neoplasms, Female - genetics | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Diagnosis, Differential | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Basal Cell Nevus Syndrome - diagnosis | Neoplastic Syndromes, Hereditary - diagnosis | von Hippel-Lindau Disease - genetics | Enchondromatosis - diagnosis | Tuberous Sclerosis - genetics | Perivascular Epithelioid Cell Neoplasms - pathology | Hamartoma Syndrome, Multiple - diagnosis | Perivascular Epithelioid Cell Neoplasms - genetics | Skin Neoplasms - genetics | Basal Cell Nevus Syndrome - genetics | Enchondromatosis - pathology | Leiomyomatosis - genetics | Perivascular Epithelioid Cell Neoplasms - diagnosis | Genital Neoplasms, Female - pathology | Enchondromatosis - genetics | Lymphangioleiomyomatosis - diagnosis | Lymphangioleiomyomatosis - genetics
Journal Article
Journal Article
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 05/2008, Volume 1131, Issue 1, pp. 155 - 184
Lymphatic disease is quite prevalent, and often not well clinically characterized. Beyond lymphedema, there is a broad array of human disease that directly or... 
chromosomal disorders | lymphangioma | lymphangioleiomyomatosis | protein-losing enteropathy (PLE) | protein‐losing enteropathy (PLE) | Chromosomal disorders | Protein-losing enteropathy (PLE) | Lymphangioleiomyomatosis | Lymphangioma | MENTAL-RETARDATION | MULTIDISCIPLINARY SCIENCES | DIFFUSE NEONATAL HEMANGIOMATOSIS | TURNERS-SYNDROME | CYSTIC ANGIOMATOSIS | INTESTINAL LYMPHANGIECTASIA | KLIPPEL-TRENAUNAY-SYNDROME | VASCULAR MALFORMATIONS | PROTEIN-LOSING ENTEROPATHY | BLEB NEVUS SYNDROME | OF-THE-LITERATURE | Parasitic Diseases - pathology | Communicable Diseases - pathology | Lymphatic Diseases - physiopathology | Lymphedema - pathology | Lymphedema - physiopathology | Humans | Lymphangioleiomyomatosis - physiopathology | Chromosome Disorders | Lymphatic Diseases - complications | Lymphangioleiomyomatosis - pathology | Subcutaneous Fat - pathology | Lymphangioma - physiopathology | Lymphedema - genetics | Protein-Losing Enteropathies - pathology | Communicable Diseases - physiopathology | Lymphatic Diseases - diagnosis | Lymphangioleiomyomatosis - complications | Protein-Losing Enteropathies - complications | Parasitic Diseases - physiopathology | Lymphatic Diseases - pathology | Parasitic Diseases - complications | Protein-Losing Enteropathies - physiopathology | Lymphangioma - pathology | Lymphatic diseases
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, p. e0126025
Lymphangioleiomyomatosis (LAM) is a rare disease leading to lungs cysts and progressive respiratory failure. Cells of unknown origin accumulate in the lungs... 
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