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Cytomegalovirus (CMV) disease is caused by human cytomegalovirus, a double-stranded DNA virus of the Herpesviridae family. While primary CMV infection is often asymptomatic in immunocompetent individuals, the virus can cause severe disease in neonates and immunocompromised patients. CMV is the most common cause of congenital viral infection in the United States, and a major pathogen in solid organ and hematopoietic stem cell transplant recipients.CMV is transmitted via bodily fluids, sexual...
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Mikulicz's disease. A case report.

I Coloma-González1, L Ruíz-García1, J Flores-Preciado1

  • 1Departamento de Órbita, Párpados y Vías Lagrimales, Hospital Dr. Luis Sánchez Bulnes, Asociación para Evitar la Ceguera IAP, México DF, México.

Archivos De La Sociedad Espanola De Oftalmologia
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PubMed
Summary
This summary is machine-generated.

Mikulicz

Keywords:
DacrioadenitisDacryoadenitisEnfermedad asociada a IgG(4)Enfermedad de MikuliczEnfermedad inflamatoria de la órbitaIgG4-related diseaseInflammatory orbital diseaseMikulicz's disease

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Area of Science:

  • Ophthalmology
  • Rheumatology
  • Pathology

Background:

  • Mikulicz's disease is a chronic inflammatory condition affecting salivary and lacrimal glands.
  • It is increasingly classified under IgG4-related diseases.
  • Diagnosis involves characteristic gland swelling and specific serological/histopathological findings.

Observation:

  • A 48-year-old male presented with bilateral salivary and lacrimal gland involvement.
  • Incisional biopsy of the lacrimal glands confirmed the diagnosis.
  • The patient experienced complete resolution following corticosteroid therapy.

Findings:

  • Mikulicz's disease presents as persistent, symmetrical swelling of lacrimal and salivary glands.
  • Elevated serum IgG4 concentrations and tissue infiltration by IgG4-positive plasma cells are key diagnostic markers.
  • This case highlights the efficacy of corticosteroids in managing the condition.

Implications:

  • This case underscores the importance of recognizing Mikulicz's disease as an IgG4-related condition.
  • Prompt diagnosis and treatment, such as corticosteroid therapy, can lead to favorable outcomes.
  • Further research into IgG4-related dacryoadenitis and sialadenitis is warranted.