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1.
Cureus ; 15(9): e46199, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37908922

ABSTRACT

Fixed-drug eruptions (FDEs) are dermatological reactions characterized by specific skin lesions triggered by certain medications. Our case reports commonly used medications that can cause drug-induced skin reactions. Chlorthalidone, a widely used diuretic, had not been prominently linked to FDEs. Here, we present the case of a 45-year-old African-American male who developed classic FDE skin lesions following the initiation of chlorthalidone therapy. This case underscores the imperative for further investigation and heightened awareness among healthcare professionals regarding chlorthalidone-associated FDEs. Findings suggest that such reactions might be more prevalent than previously acknowledged, underscoring the significance of prompt diagnosis and effective management of drug-induced skin responses. Notably, the patient's lesions showed complete resolution upon discontinuing the diuretic, reinforcing the causal relationship. This case is an essential reminder of the importance of vigilance in monitoring patients for adverse drug reactions, even in unlikely medications, such as chlorthalidone.​​​​​​.

2.
Heliyon ; 9(5): e15773, 2023 May.
Article in English | MEDLINE | ID: mdl-37215835

ABSTRACT

Curvularia rarely causes human infections despite its ubiquity in the environment. It is most associated with allergic diseases such as chronic sinusitis and allergic bronchopulmonary mycosis; however, causing a lung mass is rarely reported in the literature. We describe an interesting case of a 57-year-old man with a history of asthma and localized prostate cancer diagnosed with a Curvularia-caused lung mass that responded quickly to itraconazole.

3.
J Bronchology Interv Pulmonol ; 19(1): 57-60, 2012 Jan.
Article in English | MEDLINE | ID: mdl-23207266

ABSTRACT

Bronchoscopy and bronchoalveolar lavage (BAL) are widely accepted diagnostic procedures in various pulmonary etiologies. Complications of bronchoscopy are relatively infrequent and most often minor, namely, bleeding and infection. Pneumothorax is a rare complication of bronchoscopy with transbronchial biopsy. Bilateral pneumothorax developing after BAL without biopsy has been rarely described in the literature. A 51-year-old woman presented with symptoms suggestive of reactive airway syndrome and underwent bronchoscopy with BAL to rule out vocal cord paralysis and to investigate other potential causes of her symptoms. Immediately after BAL, she developed bilateral pneumothorax requiring chest tube placement. The pneumothorax was resolved with the chest tube and the patient recovered. However, the etiology of the pneumothorax remained unclear. We presume that cough-related increase in intrathoracic pressure might have led to interstitial air dissection and bilateral pneumothorax.


Subject(s)
Bronchial Hyperreactivity/diagnosis , Bronchoalveolar Lavage/adverse effects , Bronchoscopy/adverse effects , Cough/etiology , Pneumothorax/etiology , Biopsy , Bronchial Hyperreactivity/physiopathology , Bronchoalveolar Lavage Fluid/microbiology , Catheterization/methods , Female , Humans , Intubation, Intratracheal , Middle Aged , Pneumothorax/diagnostic imaging , Pneumothorax/therapy , Pressure/adverse effects , Radiography , Respiratory Sounds , Valsalva Maneuver/physiology , Vocal Cord Paralysis/diagnosis
4.
World J Oncol ; 3(2): 78-82, 2012 Apr.
Article in English | MEDLINE | ID: mdl-29147284

ABSTRACT

Multiple myeloma - a neoplastic proliferation of plasma cell is the second most common blood cancer. Multiple myeloma is characterized by neoplastic proliferation of the plasma cells. These cells infiltrate variety of organs. Infiltration by immature neoplastic cells and overproduction of monoclonal immunoglobulin chain is responsible for clinical manifestations of multiple myeloma. The most common clinical presentation of multiple myeloma is an asymptomatic person having anemia and elevated globulin in laboratory testing. Multiple myeloma is diagnosed by triad of > 10% marrow infiltration by plasma cells, serum/urine monoclonal protein and end organ damages. One of the common end organ damage is lytic bone lesions resulting from imbalance between osteolytic and osteoblastic activities. Lymphadenopathy and osteoblastic lesions are rare presentations of multiple myeloma - lymphadenopathy in 1% of cases with IgA subtype and osteoblastic lesions in IgE myeloma and lambda light chains. Osteoblastic multiple myeloma is a distinct entity from POEMS syndrome. IgG myeloma with kappa chain predominance is not described yet with osteoblastic lesions and lymphadenopathy. We present a rare case of IgG myeloma with kappa chain predominance that had both lymphadenopathy and osteoblastic lesions.

5.
Yale J Biol Med ; 84(1): 9-13, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21451779

ABSTRACT

Pretracheal abscess due to endotracheal intubation has not been reported in literature. We present a case of a female patient who was admitted with acute hypercapnic respiratory failure. Patient was initially managed with noninvasive ventilation but eventually was intubated after sustaining a cardiac arrest. She could not be extubated because of poor weaning parameters, so a tracheostomy was planned. During surgery, a pretracheal abscess was found with destruction of the second, third, and fourth tracheal rings and intact posterior tracheal wall. The possible risk factors, mechanism of injury, and preventive strategy of tracheal complication of intubation are discussed.


Subject(s)
Abscess/etiology , Abscess/pathology , Bacterial Infections/etiology , Bacterial Infections/pathology , Intubation, Intratracheal/adverse effects , Trachea/injuries , Trachea/microbiology , Abscess/microbiology , Aged , Fatal Outcome , Female , Humans , Respiratory Insufficiency/therapy , Risk Factors , Trachea/pathology
6.
Epigenetics ; 5(3): 241-8, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20364100

ABSTRACT

Methylation of CpG sequences in and around CGG triplet repeats in FMR1 gene has strong correlation with manifestation of the fragile X syndrome in human patients. In contrast, we have observed a lack of correlation between repeat instability and DNA methylation in three different transgenic mouse models harboring unstable CGG repeats. Further we have demonstrated that the endogenous copy of mouse Fmr1 gene remains unmethylated both in males and females. These results imply that methylation and repeat instability are independent events and raise the possibility that methylation could also result in repression of FMR1 transcription in the absence of repeat expansion.


Subject(s)
DNA Methylation/genetics , Fragile X Mental Retardation Protein/metabolism , Repetitive Sequences, Nucleic Acid , Animals , DNA Sequence, Unstable , Female , Fragile X Mental Retardation Protein/genetics , Humans , Male , Mice, Transgenic
7.
J Clin Med Res ; 2(5): 215-9, 2010 Oct 11.
Article in English | MEDLINE | ID: mdl-21629543

ABSTRACT

BACKGROUND: Proton pump inhibitors (PPIs) are used for the treatment and prophylaxis of variety of acid peptic conditions including stress ulcers. There has been a persistent practice of their inappropriate use for stress ulcer prophylaxis. Purpose of our study was to measure the inappropriate use of Intravenous Proton Pump Inhibitors for stress ulcer prophylaxis and to estimate the financial burden. METHODS: We carried out a retrospective, analytic study from July 2008 to June 2009 in internal medicine department. Hospital pharmacy records were used to identify all patients who received IV PPI during hospital stay. Seventy-five percent of records were randomly chosen (n=1104). PPI application was defined as indicated according to AGA guidelines. RESULTS: Intravenous proton pump inhibitor (IV PPI) was prescribed for 68.5% of patients without any proper indication. The estimated cost of medication for inappropriate IV PPIS use during the study year was 18337 USD. CONCLUSIONS: A more rational use of PPI will have better impact on health care cost and is likely to add to patient safety. KEYWORDS: Inappropriate use of PPI; Stress ulcer prophylaxis; Healthcare cost.

8.
Gene ; 428(1-2): 20-4, 2009 Jan 01.
Article in English | MEDLINE | ID: mdl-18976699

ABSTRACT

The expression of genes in transgenic mice is known to be influenced by the site of integration even when they carry their own promoter elements and transcription factor binding sites. The cytomegalovirus (CMV) promoter, a strong promoter often used for transgene expression in mammalian cells in culture, is known to be silenced by DNA methylation and histone deacetylation but there is no report on the role of histone methylations in its regulation. We generated two transgenic lines carrying green fluorescence protein coding gene as reporter driven by cytomegalovirus major immediate-early promoter/enhancer. We observe that silencing of CMV promoter is dependent on the site of transgene integration, except in testis, and the nature of DNA and histone methylations strongly correlate with the expression status of the reporter. We find that silenced CMV promoter interacts in vivo, with Methyl CpG binding protein 2 (MeCP2), a recruiter of histone deacetylases (HDACs) and histone (H3K9) methyl transferase. Histone H3K4methylation, the active chromatin mark, is also associated with silenced promoter, suggesting bivalent marking of the promoter and its susceptibility to reactivation on induction.


Subject(s)
Antigens, Viral/genetics , Cytomegalovirus/genetics , Epigenesis, Genetic , Gene Expression Regulation, Viral , Immediate-Early Proteins/genetics , Promoter Regions, Genetic/genetics , Animals , Antigens, Viral/metabolism , Cells, Cultured , Chromatin/metabolism , Chromatin Immunoprecipitation , CpG Islands , DNA Methylation , Gene Silencing , Green Fluorescent Proteins/metabolism , Histone Deacetylases , Histones/metabolism , Humans , Immediate-Early Proteins/metabolism , Kidney/cytology , Kidney/metabolism , Methyl-CpG-Binding Protein 2/genetics , Methyl-CpG-Binding Protein 2/metabolism , Mice , Mice, Transgenic , Regulatory Sequences, Nucleic Acid , Virus Replication
9.
J Biol Chem ; 280(10): 9450-9, 2005 Mar 11.
Article in English | MEDLINE | ID: mdl-15623522

ABSTRACT

Scaffold/matrix-associated region-1-binding protein (SMAR1) specifically interacts with the MARbeta sequence, which is located 400-bp upstream of the murine TCRbeta enhancer and is highly expressed during the DP stage of thymocyte development. To further analyze the functions of SMAR1, transgenic mice were generated that express SMAR1 in a tissue-independent manner. SMAR1-overexpressing mice exhibit severely altered frequency of the T cells expressing commonly used Vbetas (Vbeta5.1/5.2 and Vbeta8.1/8.2/8.3). The rearrangements of Vbeta5.1/5.2, Vbeta8.1/8.2/8.3 loci are also reduced in SMAR1 transgenic mice. The T cells in SMAR1 transgenic mice exhibit a mild perturbation at the early DN stage. SMAR1 transgenic mice exhibit hypercellular lymph nodes and spleen accompanied with prominent architectural defects in these organs. These results indicate that SMAR1 plays an important role in the regulation of T cell development as well as V(D)J recombination besides maintaining the architecture of the lymphoid organs.


Subject(s)
Cell Cycle Proteins/genetics , DNA-Binding Proteins/genetics , Genes, T-Cell Receptor beta , Nuclear Proteins/genetics , T-Lymphocytes/immunology , VDJ Recombinases/metabolism , Animals , DNA/genetics , DNA/isolation & purification , DNA Primers , Gene Rearrangement, T-Lymphocyte , Humans , Lymph Nodes/immunology , Mice , Mice, Transgenic , Promoter Regions, Genetic , Reverse Transcriptase Polymerase Chain Reaction , Spleen/immunology
10.
Genomics ; 80(2): 151-7, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12160728

ABSTRACT

Dynamic mutation resulting in the expansion of CGG repeats in the untranslated region (UTR) of the first exon of the FMR1 gene in humans results in fragile X syndrome. Long stretches of CGG repeats that are known to be highly unstable in humans have so far failed to show similar intergenerational instability in transgenic mice. We generated transgenic lines that show a dramatic increase from 26 to >300 repeats in three generations. One of the salient features of our transgene is the inclusion of the origin of replication of simian virus-40 (SV40), which is known to exclude nucleosomes. Three founder mice in FVB/NJ background show expansion of CGG repeats present in the transgene, supporting a postzygotic mechanism for CGG expansion that is independent of a genomic imprinting effect. We discuss here the results of analyzing one of the lines established.


Subject(s)
Mice, Transgenic , Transgenes , Trinucleotide Repeat Expansion/genetics , Trinucleotide Repeats/genetics , 3' Flanking Region , 5' Flanking Region , Animals , Female , Gene Dosage , Male , Mice , Molecular Sequence Data , Pedigree , Polymerase Chain Reaction
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