[HTML][HTML] The 2015 World Health Organization classification of lung tumors: impact of genetic, clinical and radiologic advances since the 2004 classification

WD Travis, E Brambilla, AG Nicholson, Y Yatabe… - Journal of thoracic …, 2015 - Elsevier
Abstract The 2015 World Health Organization (WHO) Classification of Tumors of the Lung,
Pleura, Thymus and Heart has just been published with numerous important changes from …

PEComa: morphology and genetics of a complex tumor family

K Thway, C Fisher - Annals of diagnostic pathology, 2015 - Elsevier
Perivascular epithelioid cell tumors, or PEComas, are mesenchymal neoplasms composed
of histologically and immunohistochemically distinctive epithelioid or spindle cells, which are …

[HTML][HTML] Renal manifestations of tuberous sclerosis complex: incidence, prognosis, and predictive factors

SK Rakowski, EB Winterkorn, E Paul, DJR Steele… - Kidney international, 2006 - Elsevier
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions
in multiple organs, frequently involving the kidney. We conducted a retrospective review of …

[HTML][HTML] Renal angiomyolipomata

JJ Bissler, JC Kingswood - Kidney international, 2004 - Elsevier
Renal angiomyolipomata. Renal angiomyolipomata can exist as an imaging curiosity or
represent a life-threatening condition. There are likely over 10 million people world-wide …

Mutation analysis of the TSC1 and TSC2 genes in Japanese patients with pulmonary lymphangioleiomyomatosis

T Sato, K Seyama, H Fujii, H Maruyama… - Journal of human …, 2002 - nature.com
Pulmonary lymphangioleiomyomatosis (LAM) is a destructive lung disease characterized by
a diffuse hamartomatous proliferation of smooth muscle cells (LAM cells) in the lungs …

Pathology of hereditary renal cell carcinoma syndromes: Tuberous sclerosis complex (TSC)

ME Machacek, CL Wu, KM Cornejo - Seminars in Diagnostic Pathology, 2024 - Elsevier
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disease characterized
by hamartomatous tumors involving multiple organs such as the brain, skin, heart, lung and …

Hereditary renal cystic disorders: imaging of the kidneys and beyond

JR Dillman, AT Trout, EA Smith, AJ Towbin - Radiographics, 2017 - pubs.rsna.org
The purpose of this article is to review the hereditary renal cystic diseases that can manifest
in children and adults, with specific attention to pathogenesis and imaging features. Various …

Pathogenesis of multifocal micronodular pneumocyte hyperplasia and lymphangioleiomyomatosis in tuberous sclerosis and association with tuberous sclerosis genes TSC1 …

H Maruyama, C Ohbayashi, O Hino… - Pathology …, 2001 - Wiley Online Library
Tuberous sclerosis (TSC) is a rare, genetically determined disorder/familial tumor syndrome,
currently diagnosed using specific clinical criteria proposed by Gomez, including the …

Loss of heterozygosity on tuberous sclerosis complex genes in multifocal micronodular pneumocyte hyperplasia

T Hayashi, T Kumasaka, K Mitani, T Yao, K Suda… - Modern …, 2010 - nature.com
Multifocal micronodular pneumocyte hyperplasia is a rare pulmonary manifestation of
tuberous sclerosis complex (TSC) that is a tumor suppressor gene disorder characterized by …

Challenges in pulmonary fibrosis· 3: Cystic lung disease

GP Cosgrove, SK Frankel, KK Brown - Thorax, 2007 - thorax.bmj.com
Cystic lung disease is a frequently encountered problem caused by a diverse group of
diseases. Distinguishing true cystic lung disease from other entities, such as cavitary lung …