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An atypical presentation of pediatric malignant spinal cord compression

Gaia, Maria João; Lopes, Vilma; Tenente, Joana; Coelho, Janine; Vila Real, Marta; Santos, Fátima

Background: Malignant spinal cord compression (MSCC) is a rare but serious complication of pediatric malignancies that can result in permanent neurologic deficits. The prognosis depends on neurological symptoms at diagnosis. Case report: A nine-year-old girl was evaluated for worsening pain in the left anterior iliac spine with one month of evolution. Over the next two days, she showed progressive gait instabil...


An atypical presentation of pediatric malignant spinal cord compression

Gaia, Maria João; Lopes, Vilma; Tenente, Joana; Coelho, Janine; Real, Marta Vila; Santos, Fátima

Background: Malignant spinal cord compression (MSCC) is a rare but serious complication of pediatric malignancies that can result in permanent neurologic deficits. The prognosis depends on neurological symptoms at diagnosis. Case report: A nine-year-old girl was evaluated for worsening pain in the left anterior iliac spine with one month of evolution. Over the next two days, she showed progressive gait instabil...


Tuberculosis in Times of COVID-19: A Diagnosis Not to Be Forgotten

Peixoto, Margarida; Tenente, Joana; Carvalho, Isabel

N/a.; N/a.

Date: 2022   |   Origin: Acta Médica Portuguesa

Dermatology clinical case

Leitão, Cátia Vilas Boas; Pereira, Isabel Ayres; Tenente, Joana; Real, Marta Vila; Oliveira, Ana; Leite, Ana Luísa

ncontinentia pigmenti is an X-linked neuroectodermal dysplasia. It is a rare genetic disease with multiorgan involvement, and hence a multidisciplinary approach is of paramount importance. Although diagnosis is based on clinical findings, genetic molecular testing can be performed to confirm diagnosis and allow future genetic counselling. The authors describe the case of a 4-month-old girl accidentally diagnose...


Neonatal cranial bone depression

Tenente, Joana; Cardoso, Ivana; Vinhas da Silva, António; Torres, Jacinto

A female preterm was admitted to the Neonatal Intensive Care Unit for late prematurity and very low weight. The physical examination was normal. On the third day of life, a hard left, non-painful parietal depression was noted, with no evidence of neurological impairment. Head computed tomography (CT) showed focal sinking of the left parietal bone posteriorly to the coronal suture. A watchful attitude was adopte...


Dermatology clinical case

Leitão, Cátia; Pereira, Isabel; Tenente, Joana; Vila-Real, Marta; Oliveira, Ana; Leite, Ana Luísa

Incontinentia pigmenti is an X-linked neuroectodermal dysplasia. It is a rare genetic disease with multiorgan involvement, and hence a multidisciplinary approach is of paramount importance. Although diagnosis is based on clinical findings, genetic molecular testing can be performed to confirm diagnosis and allow future genetic counselling. The authors describe the case of a 4-month-old girl accidentally diagnos...


Neonatal cranial bone depression

Tenente, Joana; Cardoso, Ivana; Vinhas da Silva, António; Torres, Jacinto

A female preterm was admitted to the Neonatal Intensive Care Unit for late prematurity and very low weight. The physical examination was normal. On the third day of life, a hard left, non-painful parietal depression was noted, with no evidence of neurological impairment. Head computed tomography (CT) showed focal sinking of the left parietal bone posteriorly to the coronal suture. A watchful attitude was adopte...


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