Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Language
Publication year range
1.
Rom J Intern Med ; 54(2): 129-33, 2016.
Article in English | MEDLINE | ID: mdl-27352442

ABSTRACT

We present the case of a 76 year old female patient admitted in the Department of Cardiology for physical asthenia, profuse sweating and dyspnea with orthopnea for about one month. Clinical and paraclinical assessments performed at admission confirmed the diagnosis of cardiac tamponade. Surgical intervention was performed and 400 mL of clear effusion were drained. Post-operative evolution was marked by recurrence of symptoms, requiring after 3 weeks a new drainage of 600 mL of clear effusion, and biopsy of the pericardium was performed. Pathological exam described serous pericarditis with chronic inflammatory infiltrate, xanthogranulomatous reaction intricated in the pericardium and mesothelial hyperplasia. The patient was subsequently transferred to the Department of Internal Medicine for further investigations. Physical examination showed a patient with altered general status, pallor, vesicular murmur absent in both bases, presenting cutaneous hyperpigmentation at the level of the right hemi-abdomen and hip with posterior extension, and a peripheral indurated erythematous plaque. The patient presented nodular masses of 3 cm in the right latero-cervical and bilateral axillary regions, non-adherent to the superficial structures, as well as adenopathic blocks in both inguinal regions. CT scan of the thorax and abdomen showed moderate bilateral pleuresia, minimal pericardial effusion (15 mm) and multiple adenopathies on both sides of the diaphragm. Skin biopsy was performed, as well as bone marrow aspirate and excision of a right axillary lymph node. Pathological exams and immunohistochemistry tests confirmed the diagnosis of Plasma Cells Castleman disease.


Subject(s)
Castleman Disease/diagnosis , Castleman Disease/surgery , Plasma Cells/pathology , Aged , Biopsy , Drainage , Female , Humans , Hyperpigmentation , Pericardial Effusion/diagnosis , Pericardial Effusion/surgery , Pleural Effusion/diagnosis , Pleural Effusion/surgery , Rare Diseases , Recurrence , Treatment Outcome
2.
Rom J Intern Med ; 49(2): 105-12, 2011.
Article in English | MEDLINE | ID: mdl-22303601

ABSTRACT

UNLABELLED: There are over 5000 patients with genotype 1b HCV chronic infection in Romania on national waiting lists. This allowed us to evaluate the complete and partial early virological response rates (EVRc and EVRp), as well as the factors influencing the response rates to treatment. PATIENTS: We studied 1220 treatment naive patients with HCV chronic hepatitis who started antiviral therapy during 2009. Mean age was 48 years and female gender was predominant (58%). Chronic hepatitis was documented by liver biopsy in 1129 patients (93%) or by non-invasive tests in 91 cases (7%). Most patients presented advanced liver disease (F3 + F4 Metavir = 62.3%). Viral load was over 400000 iu/mL in 61% patients and over 600000 iu/mL in 52% patients. Treatment was performed with peginterferon alpha-2a in 75.2% patients and with peginterferon alpha-2b in 24.8% patients, with comparative histology. The influence of histology, viral load, gender, age and type of peginterferon on the response rates to treatment was evaluated. RESULTS: EVRc was obtained in 76.6% patients, while 16.2% presented EVRp. From those with EVRp, 78.8% had undetectable viral load after 6 months of therapy. The nonresponder rate was 9.6%. EVRc was influenced by viral load and age, but not by fibrosis stage or type of interferon. CONCLUSIONS: We noticed a high rate of EVRc, which was not influenced by histology, gender or type of interferon. The number of nonresponders and of patients who interrupted therapy due to lack of compliance or adverse events was low.


Subject(s)
Antiviral Agents/therapeutic use , Hepacivirus/drug effects , Hepatitis C, Chronic/drug therapy , Interferon-alpha/therapeutic use , Liver Cirrhosis/drug therapy , Polyethylene Glycols/therapeutic use , Ribavirin/therapeutic use , Viral Load/drug effects , Adult , Biopsy , Disease Progression , Drug Therapy, Combination , Female , Genotype , Hepatitis C, Chronic/epidemiology , Hepatitis C, Chronic/genetics , Hepatitis C, Chronic/pathology , Humans , Interferon alpha-2 , Liver Cirrhosis/epidemiology , Liver Cirrhosis/genetics , Liver Cirrhosis/pathology , Male , Middle Aged , Prospective Studies , Recombinant Proteins/therapeutic use , Ribavirin/administration & dosage , Risk Assessment , Risk Factors , Romania/epidemiology , Time Factors , Treatment Failure , Treatment Outcome
3.
Phys Rev D Part Fields ; 53(9): 5318-5321, 1996 May 01.
Article in English | MEDLINE | ID: mdl-10020530
4.
Phys Rev D Part Fields ; 52(3): 1577-1587, 1995 Aug 01.
Article in English | MEDLINE | ID: mdl-10019378
5.
Phys Rev C Nucl Phys ; 45(2): 880-883, 1992 Feb.
Article in English | MEDLINE | ID: mdl-9967829
6.
Phys Rev C Nucl Phys ; 40(4): 1818-1821, 1989 Oct.
Article in English | MEDLINE | ID: mdl-9966171
7.
Phys Rev C Nucl Phys ; 37(5): 2209-2219, 1988 May.
Article in English | MEDLINE | ID: mdl-9954690
SELECTION OF CITATIONS
SEARCH DETAIL