Clinical course and characterisation of lymphangioleiomyomatosis in a Brazilian reference centre

Lymphangioleiomyomatosis (LAM) is a rare disease that promotes pulmonary cystic destruction and impairs pulmonary function. We aim to describe features and clinical course of LAM patients from Brazil. We described the clinical and functional features, performance in six minute walk test (6MWT), mana...

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Published inSarcoidosis, vasculitis, and diffuse lung diseases Vol. 31; no. 2; p. 129
Main Authors Baldi, Bruno Guedes, Freitas, Carolina Salim Gonçalves, Araujo, Mariana Sponholz, Dias, Olívia Meira, Pereira, Daniel Antunes Silva, Pimenta, Suzana Pinheiro, Kairalla, Ronaldo Adib, Carvalho, Carlos Roberto Ribeiro
Format Journal Article
LanguageEnglish
Published Italy 08.07.2014
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ISSN1124-0490
2532-179X
2532-179X

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Abstract Lymphangioleiomyomatosis (LAM) is a rare disease that promotes pulmonary cystic destruction and impairs pulmonary function. We aim to describe features and clinical course of LAM patients from Brazil. We described the clinical and functional features, performance in six minute walk test (6MWT), management details, survival and clinical course of 84 LAM patients followed in a Brazilian reference centre. All subjects were women, the average age at onset of symptoms was 38 years, and the average at diagnosis was 42 years. The major symptoms during the course of the disease were dyspnoea and pneumothorax. The patients experienced impaired quality of life, with worse scores in the physical and emotional domains. The most common abnormalities in pulmonary function tests were an obstructive pattern and reduced diffusion capacity, whereas a quarter of the patients had normal spirometric results. In the 6MWT, although patients had preserved exercise capacity, more than half of the patients had significant desaturation. Hormonal blockage and doxycycline were the most common treatment modalities employed in our patients. The survival probability from diagnosis was 90% at 5 years, whereas the mean annual rate of decline in FEV1 was 60 ± 78 mL. Clinical and functional features of the LAM patients from our centre are similar to those from other countries. Our sample showed preserved exercise capacity, with desaturation in the 6MWT, and impaired quality of life. Survival was similar, whereas the annual rate of decline of FEV1 was slightly lower than in recent studies.
AbstractList Lymphangioleiomyomatosis (LAM) is a rare disease that promotes pulmonary cystic destruction and impairs pulmonary function. We aim to describe features and clinical course of LAM patients from Brazil. We described the clinical and functional features, performance in six minute walk test (6MWT), management details, survival and clinical course of 84 LAM patients followed in a Brazilian reference centre. All subjects were women, the average age at onset of symptoms was 38 years, and the average at diagnosis was 42 years. The major symptoms during the course of the disease were dyspnoea and pneumothorax. The patients experienced impaired quality of life, with worse scores in the physical and emotional domains. The most common abnormalities in pulmonary function tests were an obstructive pattern and reduced diffusion capacity, whereas a quarter of the patients had normal spirometric results. In the 6MWT, although patients had preserved exercise capacity, more than half of the patients had significant desaturation. Hormonal blockage and doxycycline were the most common treatment modalities employed in our patients. The survival probability from diagnosis was 90% at 5 years, whereas the mean annual rate of decline in FEV1 was 60 ± 78 mL. Clinical and functional features of the LAM patients from our centre are similar to those from other countries. Our sample showed preserved exercise capacity, with desaturation in the 6MWT, and impaired quality of life. Survival was similar, whereas the annual rate of decline of FEV1 was slightly lower than in recent studies.
Lymphangioleiomyomatosis (LAM) is a rare disease that promotes pulmonary cystic destruction and impairs pulmonary function. We aim to describe features and clinical course of LAM patients from Brazil.BACKGROUND AND OBJECTIVELymphangioleiomyomatosis (LAM) is a rare disease that promotes pulmonary cystic destruction and impairs pulmonary function. We aim to describe features and clinical course of LAM patients from Brazil.We described the clinical and functional features, performance in six minute walk test (6MWT), management details, survival and clinical course of 84 LAM patients followed in a Brazilian reference centre.METHODSWe described the clinical and functional features, performance in six minute walk test (6MWT), management details, survival and clinical course of 84 LAM patients followed in a Brazilian reference centre.All subjects were women, the average age at onset of symptoms was 38 years, and the average at diagnosis was 42 years. The major symptoms during the course of the disease were dyspnoea and pneumothorax. The patients experienced impaired quality of life, with worse scores in the physical and emotional domains. The most common abnormalities in pulmonary function tests were an obstructive pattern and reduced diffusion capacity, whereas a quarter of the patients had normal spirometric results. In the 6MWT, although patients had preserved exercise capacity, more than half of the patients had significant desaturation. Hormonal blockage and doxycycline were the most common treatment modalities employed in our patients. The survival probability from diagnosis was 90% at 5 years, whereas the mean annual rate of decline in FEV1 was 60 ± 78 mL.RESULTSAll subjects were women, the average age at onset of symptoms was 38 years, and the average at diagnosis was 42 years. The major symptoms during the course of the disease were dyspnoea and pneumothorax. The patients experienced impaired quality of life, with worse scores in the physical and emotional domains. The most common abnormalities in pulmonary function tests were an obstructive pattern and reduced diffusion capacity, whereas a quarter of the patients had normal spirometric results. In the 6MWT, although patients had preserved exercise capacity, more than half of the patients had significant desaturation. Hormonal blockage and doxycycline were the most common treatment modalities employed in our patients. The survival probability from diagnosis was 90% at 5 years, whereas the mean annual rate of decline in FEV1 was 60 ± 78 mL.Clinical and functional features of the LAM patients from our centre are similar to those from other countries. Our sample showed preserved exercise capacity, with desaturation in the 6MWT, and impaired quality of life. Survival was similar, whereas the annual rate of decline of FEV1 was slightly lower than in recent studies.CONCLUSIONSClinical and functional features of the LAM patients from our centre are similar to those from other countries. Our sample showed preserved exercise capacity, with desaturation in the 6MWT, and impaired quality of life. Survival was similar, whereas the annual rate of decline of FEV1 was slightly lower than in recent studies.
Author Freitas, Carolina Salim Gonçalves
Araujo, Mariana Sponholz
Carvalho, Carlos Roberto Ribeiro
Pimenta, Suzana Pinheiro
Pereira, Daniel Antunes Silva
Dias, Olívia Meira
Kairalla, Ronaldo Adib
Baldi, Bruno Guedes
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  organization: Pulmonary Division, Heart Institute (InCor), Hospital das Clínicas, University of Sao Paulo Medical School, Sao Paulo, Brazil. bruno.guedes2@terra.com.br
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SubjectTerms Adult
Brazil
Disease Progression
Doxycycline - therapeutic use
Emotions
Exercise Test
Exercise Tolerance
Female
Forced Expiratory Volume
Hormone Antagonists - therapeutic use
Humans
Lung - physiopathology
Lymphangioleiomyomatosis - diagnosis
Lymphangioleiomyomatosis - drug therapy
Lymphangioleiomyomatosis - mortality
Lymphangioleiomyomatosis - physiopathology
Lymphangioleiomyomatosis - psychology
Male
Middle Aged
Predictive Value of Tests
Quality of Life
Respiratory Function Tests
Retrospective Studies
Severity of Illness Index
Surveys and Questionnaires
Survival Analysis
Time Factors
Treatment Outcome
Title Clinical course and characterisation of lymphangioleiomyomatosis in a Brazilian reference centre
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