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Isolated Congenital Asplenia in an Asymptomatic Patient: A Very Rare Diagnosis

Dinis-Ferreira, Sofia; Lemos, Cláudia; Caldeira, Mónica; Homem-Costa, Miguel; Brazão, Maria da Luz; Aveiro, Fernando

Isolated congenital asplenia is a rare condition that mostly manifests in the early years, usually due to fatal systemic infections. In this paper, however, we present a case of a 36-year-old asymptomatic patient who was referred for suspected hyposplenism, with no history of splenectomy. There were no significant changes on physical examination. Blood analysis revealed leukocytosis and thrombocytosis as well a...


Isolated Congenital Asplenia in an Asymptomatic Patient: A Very Rare Diagnosis

Dinis-Ferreira, Sofia; Lemos, Cláudia; Caldeira, Mónica; Homem-Costa, Miguel; da Luz Brazão, Maria; Aveiro, Fernando

Isolated congenital asplenia is a rare condition that mostly manifests in the early years, usually due to fatal systemic infections. In this paper, however, we present a case of a 36-year-old asymptomatic patient who was referred for suspected hyposplenism, with no history of splenectomy. There were no significant changes on physical examination. Blood analysis revealed leukocytosis and thrombocytosis as well a...


Kikuchi-Fujimoto Syndrome: A Rare Entity to Consider

Raposo André, Diogo; Vicente, Filipa; Chaves, Jéssica; Caldeira, Mónica; Jacinto, Fernando; Chaves, António José; Brazão, Maria Da Luz

Kikuchi-Fujimoto disease (KFD) is a rare, benign, necrotizing lymphadenitis of unknown aetiology with good prognosis. It is characterized by c, cand fever. Surgical excision of the c, histopathological study and immunophenotyping are crucial for diagnosis.


Uma complicaçao rara de nefrolitíase

Nóbrega, Catarina; Caldeira, Mónica; Brazão, Maria da Luz


Diabetes insípida… um indício para o diagnóstico de sarcoidose

Resende, Eduarda; Caldeira, Mónica; Freitas, Ema; Sá, Maritza; Ferreira, Margarida; Abreu, Silvestre

O atingimento do sistema nervoso central pela sarcoidose é uma entidade rara, presente em cerca de 5% dos casos. A diabetes insípida, o hipogonadismo e a hiperprolactinemia são as manifestac¸ ões endócrinas mais comuns. Apresenta-se o caso de um doente do sexo masculino, caucasiano, 40 anos de idade, com quadro clínico com evoluc¸ ão de 6 meses caracterizado por sede excessiva e preferência por bebidas frias, c...


Chronic Tophaceous Gout

Spínola, Adelaide; Caldeira, Mónica; Dias, Graça

Keywords: Hyperuricemia; Gout; Arthritis, Rheumatoid.; Palavras-chave: Hiperuricemia; Gota; Artrite Reumatoide.

Data: 2014   |   Origem: Acta Médica Portuguesa

Pneumo-encephalocele

Caldeira, Mónica; Perneta, Filipe; Freitas, Luís

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Data: 2013   |   Origem: Acta Médica Portuguesa

Esophageal Perforation with Acute Mediastínitis

Caldeira, Mónica; Perneta, Filipe; Freitas, Luís; Caldeira Ferreira, António; Reis Frazão, Luís

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Data: 2013   |   Origem: Acta Médica Portuguesa

Unilateral gynecomastia caused by a calcium-channel blocker

Perneta, Filipe; Caldeira, Mónica; Ferreira, António Caldeira


Bechcet´s Disease : an old illness with a new treatment?

Perneta, Filipe; Caldeira, Mónica; Chaves, Susana; Jardim, Margarida; Miranda, Rubina; Câmara, Margarida; Reis, Maria da Luz


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