A Case of Cryptococcosis involving Lung and CNS without Underlying Disease.
10.4046/trd.1995.42.4.618
- Author:
Min Su LEE
1
;
Sang Seon PARK
;
Young Il KOH
;
An Soo JANG
;
Sung Chul LIM
;
Ju Yeoul YANG
;
Hyung Kwan PARK
;
Hyun Joo NA
;
Young Chul KIM
;
In Seon CHOI
;
Kyung Ok PARK
Author Information
1. Department of Internal Medicine, Chonnam University, College of Medicine, Kwangju, Korea.
- Publication Type:Case Report
- Keywords:
Cryptococcosis;
Lung and CNS invasion
- MeSH:
Amphotericin B;
Biopsy, Fine-Needle;
Blood Glucose;
Brain;
Central Nervous System;
Cerebellum;
Columbidae;
Complement System Proteins;
Cryptococcosis*;
Cryptococcus neoformans;
Diagnosis;
Female;
Fluconazole;
Follow-Up Studies;
Frontal Lobe;
Fungi;
Headache;
HIV;
HIV Infections;
Humans;
Immunoglobulins;
Inhalation;
Lung*;
Magnetic Resonance Imaging;
Pneumonia;
Prostate;
Sarcoidosis;
Skin;
Soil;
Spores;
Sputum;
T-Lymphocyte Subsets;
Thorax;
Tomography, X-Ray Computed
- From:Tuberculosis and Respiratory Diseases
1995;42(4):618-623
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Cryptococcosis is a systemic mycosis that most often involves the lungs and central nervous system and, less frequently, the skin, skeletal system, and prostate gland. Cryptococcus neoformans, the causative organism, is a yeastlike round or oval fungus, 4 to 6microm in diameter, which is surrounded by a polysaccharide capsule and reproduces by budding and found in soil and other enviromental areas, especially those contaminated by pigeon droppings. Humans and aninmals acquire infection after inhalation of aerosolized spores. Condition or factors that predispose to cryptococcosis include corticosteroid therapy, lymphoreticular malignancies, HIV infection, and sarcoidosis etc. We discribed a case of cryptococcosis involving lung and CNS coincidently without specific underlying disease and the literature on subject were reviewed. A fifty-six year-old previously healthy female presented with headache of 3 months of duration. She had no history suggesting immunologic suppression and we could not find any abnormal laboratory findings including blood sugar, serum immunoglobulin and complement level, HIV antibody, and T cell subsets. Chest roentgenogram and CT scan showed a solitary soft tissue mass in LUL with distal pneumonitis. Brain MRI showed granulomatous lesion in cerebellum and parasagittal cortex of right frontal lobe. The diagnosis was made by bronchoscopic brushing cytology, transthoracic fine needle aspiration, and sputum OH mount and culture. She was treated 6 weeks course of Amphotericin B and switched to oral fluconazole therapy for 3 months. Her symptoms and X-ray findings were improved gradually and she is now under regular clinical follow up.
