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2.
Dermatol Online J ; 17(6): 4, 2011 Jun 15.
Article in English | MEDLINE | ID: mdl-21696684

ABSTRACT

Superior vena cava syndrome, which occurs in approximately 15,000 persons in the United States annually, consists of a collection of symptoms and signs resulting from the obstruction of the superior vena cava (SVC). An early and prominent symptom of this condition is a constellation of superficial, dilated, vertically oriented and tortuous cutaneous venules or veins above the ribcage margins, often presenting as a blanchable violaceous eruption. Herein, we report a case of superior vena cava syndrome diagnosed in our dermatology clinic.


Subject(s)
Carcinoma, Small Cell/complications , Lung Neoplasms/complications , Superior Vena Cava Syndrome/diagnosis , Superior Vena Cava Syndrome/etiology , Aged , Carcinoma, Small Cell/diagnostic imaging , Dexamethasone/analogs & derivatives , Dexamethasone/therapeutic use , Dyspnea/etiology , Exanthema/diagnosis , Fatal Outcome , Glucocorticoids/therapeutic use , Hemoptysis/etiology , Humans , Lung Neoplasms/diagnostic imaging , Male , Oxygen/therapeutic use , Radiography , Superior Vena Cava Syndrome/therapy
3.
Dermatol Online J ; 12(5): 8, 2006 Sep 08.
Article in English | MEDLINE | ID: mdl-16962023

ABSTRACT

An 84-year-old man presented with an enlarging bluish, painless subcutaneous nodule on the glabella. The lesion had been excised 4 years prior and was diagnosed as chondroid syringoma, but had gradually regrown. The recurrent lesion was treated by surgical re-excision. Histopathological examination was again consistent with chondroid syringoma, and showed the following: 1) a chondroid matrix, 2) tubuloalveolar structures lined by a double epithelium, 3) ductal structures lined by a single epithelium, 4) nests of polygonal cells, and 5) the presence of keratinous cysts. Chondroid syringoma is a rare mixed tumor of the skin that was first described by Hirsch and Helwig. Characteristically, it is composed of a proliferation of epithelial cells set in a myxoid and chondroid matrix. Although chondroid syringomas are predominantly benign, malignant forms have been reported.


Subject(s)
Adenoma, Pleomorphic/pathology , Facial Neoplasms/pathology , Neoplasm Recurrence, Local/pathology , Sweat Gland Neoplasms/pathology , Aged, 80 and over , Humans , Male
4.
Cutis ; 71(4): 303-6, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12729095

ABSTRACT

Pemphigus erythematosus (PE) is an autoimmune blistering disease combining features of pemphigus foliaceus (PF) and systemic lupus erythematosus (SLE). We report a case of PE associated with anti-double-stranded DNA (anti-dsDNA), anti-Smith (anti-Sm), anti-Ro (anti-SSA), and antiribonucleoprotein (anti-RNP) antibodies. This case required extensive immunosuppressive therapy. We treated our patient with a combination of systemic steroids, intramuscular gold injections, azathioprine, and hydroxychloroquine. The patient's response was complete remission--evaluated clinically, serologically, and immunohistochemically.


Subject(s)
Antibodies, Antinuclear/blood , Antigens, Nuclear/blood , Autoantibodies/blood , Lupus Erythematosus, Systemic/immunology , Pemphigus/immunology , Adult , Female , Humans , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/drug therapy , Lupus Erythematosus, Systemic/pathology , Pemphigus/complications , Pemphigus/drug therapy , Pemphigus/pathology , Skin/pathology
5.
EMBO J ; 21(1-2): 31-42, 2002 Jan 15.
Article in English | MEDLINE | ID: mdl-11782423

ABSTRACT

INI1 (integrase interactor 1)/hSNF5 is a component of the mammalian SWI/SNF complex and a tumor suppressor mutated in malignant rhabdoid tumors (MRT). We have identified a nuclear export signal (NES) in the highly conserved repeat 2 domain of INI1 that is unmasked upon deletion of a downstream sequence. Mutation of conserved hydrophobic residues within the NES, as well as leptomycin B treatment abrogated the nuclear export. Full-length INI1 specifically associated with hCRM1/exportin1 in vivo and in vitro. A mutant INI1 [INI1(1-319) delG950] found in MRT lacking the 66 C-terminal amino acids mislocalized to the cytoplasm. Full-length INI1 but not the INI1(1-319 delG950) mutant caused flat cell formation and cell cycle arrest in cell lines derived from MRT. Disruption of the NES in the delG950 mutant caused nuclear localization of the protein and restored its ability to cause cell cycle arrest. These observations demonstrate that INI1 has a masked NES that mediates regulated hCRM1/exportin1-dependent nuclear export and we propose that mutations that cause deregulated nuclear export of the protein could lead to tumorigenesis.


Subject(s)
Active Transport, Cell Nucleus/physiology , DNA-Binding Proteins/metabolism , Karyopherins/metabolism , Receptors, Cytoplasmic and Nuclear , Rhabdoid Tumor/etiology , Rhabdoid Tumor/genetics , Active Transport, Cell Nucleus/drug effects , Amino Acid Sequence , Base Sequence , Binding Sites , Cell Cycle , Cell Size/genetics , Cell Transformation, Neoplastic/genetics , Chromosomal Proteins, Non-Histone , DNA, Neoplasm/genetics , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/genetics , Fatty Acids, Unsaturated/pharmacology , HeLa Cells , Humans , Molecular Sequence Data , Mutation , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , SMARCB1 Protein , Sequence Deletion , Sequence Homology, Amino Acid , Transcription Factors , Exportin 1 Protein
6.
Chaos ; 1(3): 343-345, 1991 Oct.
Article in English | MEDLINE | ID: mdl-12779931

ABSTRACT

A particularly simple chaotic nonequilibrium open system with two Cartesian degrees of freedom, characterized by two distinct temperatures T(x) and T(y), is introduced. The two temperatures are maintained by Nose-Hoover canonical-ensemble thermostats. Both the equilibrium (no net heat transfer) and nonequilibrium (dissipative) Lyapunov spectra are characterized for this simple system.

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