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1.
Res Rep Trop Med ; 15: 73-78, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-39070289

RESUMEN

Background: Ascaris lumbricoides is a common infectious parasite of the gastrointestinal tract worldwide, but the invasion of the pleural cavity is rare. Case Report: A 45-year-old man from Eastern Sudan presented to the emergency department complaining of breathlessness, cough stained with blood, and chest pain one month before his presentation. Also, he complained of high-grade fever for two weeks associated with sweating. Diagnosis of hydropneumothorax was made and a chest tube was inserted, two days later we found three adult A. lumbricoides worms in the chest drain. Conclusion: The patient was treated with Albendazole 200 mg, orally twice, daily for seven days, he improved and was referred to a cardiothoracic surgeon for more assessment. Our study highlights that internal medicine specialists should know about pleural ascariasis when patients present with respiratory signs and symptoms, especially in A. lumbricoides endemic regions like Eastern Sudan.

2.
J Med Case Rep ; 11(1): 135, 2017 May 14.
Artículo en Inglés | MEDLINE | ID: mdl-28501028

RESUMEN

BACKGROUND: Castleman disease is a rare lymphoproliferative disorder presenting with localized or disseminated lymphadenopathy and systemic manifestations. It can be categorized in numerous ways, such as unicentric versus multicentric, histopathological variants (hyaline-vascular, plasma cell, and mixed), or subtypes based on causative viral infections (human immunodeficiency virus, human herpesvirus-8, or Kaposi sarcoma herpesvirus). Presentation ranges from asymptomatic to symptoms involving multiple organs. Even though the exact mechanism of pathogenesis is unknown, treatment is directed toward possible etiologies such as interleukin-6, cluster of differentiation 20, and viral agents. CASE PRESENTATION: A 36-year-old Sri Lankan woman presented with generalized body swelling and foamy urine of 2 weeks' duration. Examination revealed pallor; generalized edema; axillary, cervical, and inguinal lymphadenopathy; hypertension; and hepatomegaly. Investigations showed bicytopenia, nephrotic range proteinuria with hypoalbuminemia, hypogammaglobulinemia, and features of hyaline-vascular type Castleman disease in a lymph node biopsy. She was managed with rituximab and had good clinical improvement. CONCLUSIONS: Castleman disease has a broad spectrum of clinical manifestations, disease pathogeneses, and associations and/or complications. Medical professionals need to be familiar with this spectrum because timely diagnosis and aggressive targeted therapy are the cornerstones of managing these patients.


Asunto(s)
Enfermedad de Castleman/diagnóstico , Diarrea/diagnóstico , Enfermedades Hereditarias del Ojo/diagnóstico , Hepatomegalia/patología , Enfermedades Intestinales/diagnóstico , Linfadenopatía/patología , Proteinuria/patología , Anomalías Cutáneas/diagnóstico , Enfermedades Vasculares/diagnóstico , Adulto , Antihipertensivos/uso terapéutico , Enfermedad de Castleman/complicaciones , Enfermedad de Castleman/tratamiento farmacológico , Diarrea/complicaciones , Diarrea/tratamiento farmacológico , Diuréticos/uso terapéutico , Enfermedades Hereditarias del Ojo/complicaciones , Enfermedades Hereditarias del Ojo/tratamiento farmacológico , Femenino , Hepatomegalia/etiología , Humanos , Factores Inmunológicos/uso terapéutico , Enfermedades Intestinales/complicaciones , Enfermedades Intestinales/tratamiento farmacológico , Linfadenopatía/etiología , Proteinuria/etiología , Rituximab/uso terapéutico , Biopsia del Ganglio Linfático Centinela , Anomalías Cutáneas/complicaciones , Anomalías Cutáneas/tratamiento farmacológico , Resultado del Tratamiento , Enfermedades Vasculares/complicaciones , Enfermedades Vasculares/tratamiento farmacológico
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