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Cryptoccocal menigitis as a primary manifestation in a patient with intestinal lymphangictasia
Shaik Afshan Jabeen1, Aruna Murthy, Rukmini Mridula Kandadai
1Department of Neurology, Nizam's Institute of Medical Sciences, Hyderabad, Andhra Pradesh, India.
Abstract:
Opportunistic infections usually occur in patients with an immunocompromised state, and can be severe. Cryptoccocal meningitis is a fatal condition if left untreated, and is usually found in such patients. We report the case of an adult patient with cryptoccocal meningitis secondary to intestinal lymphangiectasia. A 30 year old female was admitted to our hospital for meningitis. Biochemical and radiological investigations were performed. A cerebrospinal fluid latex agglutination test showed positive cryptoccocal antigen. In addition, there were features of humoral and cell mediated immunity deficiency (lymphopenia, hypoalbuminemia, hypogammaglobulinemia), with a negative human immunodeficiency virus (HIV) test by enzyme linked immunosorbent assay and polymerase chain reaction. An upper gastroduodenoscopy was performed, which showed multiple lymphangiectasias, and a biopsy confirmed the diagnosis of primary intestinal lymphangiectasia (PIL). The patient was treated with intravenous amphotericin B and oral flucytosine, and the meningitis resolved. PIL should be suspected in patients with cryptoccocal meningitis, combined with humoral and cell mediated immunity with a negative HIV test. The management issues, in addition to antifungal therapy, include nutritional supplements for the protein losing enteropathy.
Insights
Cryptococcal meningitis, a severe opportunistic infection, can occur in patients with primary intestinal lymphangiectasia (PIL). Early diagnosis and treatment of PIL are crucial for managing this potentially fatal condition.
Area of Science:
- Infectious Diseases
- Gastroenterology
- Immunology
Background:
- Opportunistic infections, such as cryptococcal meningitis, typically affect immunocompromised individuals.
- Primary intestinal lymphangiectasia (PIL) is a rare disorder characterized by impaired lymphatic drainage in the small intestine, leading to protein-losing enteropathy and potential immune deficiencies.
Observation:
- A case of cryptococcal meningitis in an immunocompetent adult patient is presented.
- The patient exhibited lymphopenia, hypoalbuminemia, and hypogammaglobulinemia, with negative Human Immunodeficiency Virus (HIV) tests.
- Diagnostic investigations revealed primary intestinal lymphangiectasia (PIL) as the underlying cause.
Findings:
- Cerebrospinal fluid analysis confirmed cryptococcal meningitis via a positive latex agglutination test.
- Gastrointestinal endoscopy and biopsy confirmed the diagnosis of primary intestinal lymphangiectasia (PIL).
- The patient successfully responded to antifungal treatment with amphotericin B and flucytosine.
Implications:
- Primary intestinal lymphangiectasia (PIL) should be considered in the differential diagnosis of cryptococcal meningitis, especially in patients with unexplained immune deficiencies and negative HIV tests.
- Management requires a dual approach: aggressive antifungal therapy for meningitis and nutritional support for protein-losing enteropathy associated with PIL.
- This case highlights the complex interplay between gastrointestinal disorders and opportunistic infections, emphasizing the need for a comprehensive diagnostic workup.
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