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1.
Int. j. cardiovasc. sci. (Impr.) ; 35(3): 410-418, May-June 2022. graf
Article in English | LILACS | ID: biblio-1375650

ABSTRACT

Abstract An acute respiratory syndrome caused by SARS-CoV2 was declared a pandemic by the World Health Organization. Current data in the world and in Brazil show that approximately 40% of patients who died have some type of cardiac comorbidity. There are also robust reports showing an increase in IL-6 / IL-1B / TNF-alpha and the presence of lymphopenia in patients with COVID-19. Our team and others have shown that increased cytokines are the link between arrhythmias/Left ventricular dysfunction and the immune system in different diseases. In addition, it has been well demonstrated that lymphopenia can not only be a good marker, but also a factor that causes heart failure. Thus, the present review focused on the role of the immune system upon the cardiac alterations observed in the SARS-CoV2 infection. Additionally, it was well described that SARS-CoV-2 is able to infect cardiac cells. Therefore, here it will be reviewed in deep.


Subject(s)
Arrhythmias, Cardiac/complications , SARS-CoV-2/pathogenicity , COVID-19/complications , Heart Failure/etiology , Myocardium/immunology , Arrhythmias, Cardiac/physiopathology , Cytokines , Cytokines/immunology , Coronavirus/pathogenicity , Ventricular Dysfunction, Left/physiopathology , Myocytes, Cardiac/pathology , Severe Acute Respiratory Syndrome , Heart Failure/complications , Lymphopenia/complications
2.
Medicina (B.Aires) ; 72(5): 435-438, oct. 2012. ilus
Article in Spanish | LILACS | ID: lil-657543

ABSTRACT

El síndrome de Sjögren es una enfermedad autoinmune caracterizada por disminución de las secreciones de las glándulas exocrinas; puede presentar también diversas alteraciones hemáticas, entre ellas linfopenia. Presentamos el caso de un varón de 28 años que consultó por cefalea de un mes de evolución a la que se agregaron en las últimas 48 horas vómitos y fiebre. Presentaba lesiones en piel de tronco y cara; no tenía rigidez de nuca. Se demostró infección por Histoplasma capsulatum var. capsulatum en piel y líquido cefalorraquídeo, linfopenia, anticuerpos anti Ro-SSA positivos, baja concentración del trazador en centellograma de glándulas salivales e infiltración linfocitaria en glándulas salivales, lo que permitió confirmar al diagnóstico de síndrome de Sjögren. El tratamiento con anfotericina liposomal e itraconazol mejoró el cuadro clínico. Comunicamos este caso para referir que una infección oportunista, como la histoplasmosis diseminada, puede ser una forma poco común de presentación del síndrome de Sjögren.


Sjögren's syndrome is an autoimmune disease characterized by decreased exocrine gland secretions; patients may also present several hematological abnormalities, like lymphopenia. We describe the case of a 28 year old man who complained of headache a month of duration, with fever and vomiting in the last 48 hours. He also presented skin lesions on trunk and face, without neck stiffness. The diagnosis of duration infection was confirmed by culture from the skin biopsy and spinal fluid specimens; in addition, the presence of lymphopenia, positive anti Ro-SSA antibodies, poor concentration of the tracer in scintigraphy and lymphocytic infiltration in salivary glands confirmed the diagnosis of Sjögren's syndrome. The patient was successfully treated with liposomal amphotericin and itraconazole. We report this case to emphasize that opportunistic infections, such as disseminated histoplasmosis, may be an uncommon clinical presentation of Sjögren's syndrome.


Subject(s)
Adult , Humans , Male , Histoplasma , Histoplasmosis/complications , Lymphopenia/complications , Sjogren's Syndrome/complications , Amphotericin B/therapeutic use , Antifungal Agents/therapeutic use , Histoplasmosis/drug therapy , Itraconazole/therapeutic use , Lymphopenia/drug therapy , Sjogren's Syndrome/drug therapy
3.
Indian J Med Microbiol ; 2012 Jul-Sept; 30(3): 367-370
Article in English | IMSEAR | ID: sea-143990

ABSTRACT

Idiopathic CD4 lymphocytopenia (ICL) is a rare disorder which is often diagnosed as HIV-negative AIDS in the light of poor immunity and AIDS-defining illnesses. We present a case of a 50-year-old male who presented with a midline posterior fossa tumour with ICL diagnosed as cerebellar cryptococcoma.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Central Nervous System Fungal Infections/diagnosis , Central Nervous System Fungal Infections/microbiology , Central Nervous System Fungal Infections/pathology , Cerebellum/pathology , Cerebellum/diagnostic imaging , Cryptococcosis/diagnosis , Cryptococcosis/microbiology , Cryptococcosis/pathology , Cryptococcus neoformans/isolation & purification , Humans , Lymphopenia/complications , Lymphopenia/diagnosis , Male , Middle Aged , Tomography, X-Ray Computed
4.
Indian Pediatr ; 2008 Feb; 45(2): 148-50
Article in English | IMSEAR | ID: sea-14479

ABSTRACT

Autoimmune Lymphoproliferative syndrome (ALPS) is an inherited disorder manifesting with autoimmune cytopenia, lymphadenopathy and splenomegaly. The differential diagnosis includes infections, autoimmune disorders or malignancies. The disease is characterized by accumulation of double negative (CD3+ CD4- CD8-) T cells (DNT) in the peripheral blood. We describe a case and review the literature.


Subject(s)
CD3 Complex/immunology , CD4 Antigens/immunology , CD8 Antigens/immunology , Autoantibodies/immunology , Child , Comorbidity , Diagnosis, Differential , Humans , Lymphatic Diseases/complications , Lymphopenia/complications , Male , Splenomegaly/complications , Syndrome
5.
Yonsei Medical Journal ; : 173-176, 2005.
Article in English | WPRIM | ID: wpr-57190

ABSTRACT

Cryptococcus neoformans commonly causes opportunistic infections in immunocompromised patients, especially in patients with AIDS. CD4+ T-lymphocytopenia in AIDS indicates an increased risk of opportunistic infection and a decline in immunological function. Idiopathic CD4 T-lymphocytopenia (ICL) is characterized by depletions in the CD4+ T-cell subsets, without evidence of HIV infection. Immunodeficiency can exist in the absence of laboratory evidence of HIV infection, and T-cell subsets should be evaluated in patients who present with unusual opportunistic infections. We report a case of pulmonary cryptococcosis and lung cancer in a patient with persistently low CD4+ cell counts, without evidence of HIV infection.


Subject(s)
Aged , Humans , Male , CD4 Lymphocyte Count , CD4-Positive T-Lymphocytes/pathology , Carcinoma, Non-Small-Cell Lung/complications , Cryptococcosis/complications , Lung Neoplasms/complications , Lymphopenia/complications
6.
Rev. chil. infectol ; 16(4): 299-304, 1999. tab
Article in Spanish | LILACS | ID: lil-274511

ABSTRACT

Presentamos una serie de 43 pacientes con neumonía por P. carinii confirmada ya sea por anatomía patológica y/o RPC, destacando como patología de base más frecuente el SIDA, pero también se pesquisaron casos en pacientes con otras inmunodeficiencias, leucemia linfoblástica aguda, tratamiento inmunosupresor y linfopenia idiopática. En los pacientes infectados por VIH la evolución del cuadro fue larvada mientras que en los pacinetes leucémicos la presentación clínica del cuadro fue más agresiva. Destacó la tríada sintomática de fiebre, tos y disnea como los hallazgos clínicos más frecuentes, junto a una elevación constante de LDH y un recuento de CD4 inferior a 200 células/mm3. La mayoría de los pacientes presentó un patrón radiológico de tipo retículo nodular, aunque se evidenciaron también condensaciones y radiografías de tórax normales. La mayoría de los pacientes presentó una evolución clínica favorable con pocas reacciones adversas severas a cotrimoxazol, pero sí más frecuentes a pentamidina intravenosa. En el subgrupo de pacientes admitidos en UCI se observó una elevada letalidad


Subject(s)
Humans , Female , Male , Adolescent , Adult , Middle Aged , AIDS-Related Opportunistic Infections/diagnosis , Pneumonia, Pneumocystis/etiology , Clinical Evolution , Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications , Lymphopenia/complications , Pneumonia, Pneumocystis/diagnosis , Pneumonia, Pneumocystis/drug therapy , Pneumonia, Pneumocystis/epidemiology , Retrospective Studies
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