Browsing by Author "Veiga, M"
Now showing 1 - 5 of 5
Results Per Page
Sort Options
- Distrofia Simpática ReflexaPublication . Oliveira, M; Veiga, M; Cantinho, GA Distrofia Simpática Reflexa é rara em pediatria. É uma síndrome complexa de dor regional, de causa desconhecida, geralmente pós-traumática, com disfunção músculo-esquelética, vascular e da pele: dor intensa persistente de um membro associada a alterações vasculares e sensoriais, incapacidade física e disfunção psico-social. O diagnóstico é essencialmente clínico, baseado num alto índice de suspeita. Na criança e adolescente há aspectos distintos dos do adulto. Excessivos testes diagnósticos podem agravar o quadro. A cintigrafia óssea é um exame útil. O tratamento da dor é controverso, não específico. As técnicas de fisioterapia e relaxamento dão algum alívio. Deve ser tratada a depressão. Esta síndrome inclui a fibromialgia e a síndrome de dor regional complexa tipo I. Apresenta-se o caso clínico de uma adolescente com quadro de dor, arrefecimento, palidez e impotência funcional do membro inferior após traumatismo minor. Tinha antecedentes de depressão. A cintigrafia óssea foi um exame decisivo. A terapêutica com gabapentina, vitamina C, fisioterapia e psicoterapia levaram à remissão persistente dos sintomas
- Labyrinthine Enhancement on 3D Black Blood MR Images of the Brain As an Imaging Biomarker for Cisplatin Ototoxicity in (Lung) Cancer PatientsPublication . Veiga, M; Kuhweide, R; Demaerel, V; De Pauw, R; De Foer, B; Casselman, JPurpose: Cancer patients treated with platinum-based chemotherapy can present with ototoxicity symptoms. The purpose of this work is to report the imaging features related to cisplatin ototoxicity. Methods: Between December 2015 and March 2019, a cohort of 96 consecutive patients with lung cancer was selected. Only patients who received cisplatin chemotherapy and underwent an imaging protocol consisting of a Gd-enhanced 3D-BB and 3D-T1W sequence, as well as T2W sequence to exclude metastases, were included. Labyrinthine enhancement was assessed, and all findings regarding the auditory and vestibular function were retrieved from the clinical files. Results: Twenty-one patients met the inclusion criteria. The Gd-enhanced 3D-BB images were used to divide them into the labyrinth enhancement group (LEG) and the labyrinth non-enhancement group (LNEG). None of these patients demonstrated enhancing regions on the 3D-T1W images. The labyrinthine fluid remained high on the T2 images in all patients, excluding metastases. The LEG consisted of 6 patients. The cochlea and semicircular canals were the most frequently affected regions. All the LEG patients that presented with hearing loss (4/6) had cochlear enhancement. Patients with normal hearing had no cochlear enhancement. Five patients (5/6) showed vestibular enhancement. Four of these patients had vestibular symptoms. Conclusion: Labyrinthine enhancement as an imaging feature related to cisplatin ototoxicity is unreported. This study demonstrates a correlation between hearing loss and cochlear enhancement and also between vestibular impairment and vestibular/semicircular enhancement on 3D-BB images, which remained invisible on the 3D-T1W images. The labyrinthine enhancement on 3D-BB images in the presence of normal signal intensity of the intralabyrinthine fluid can be used as an imaging biomarker for cisplatin toxicity in daily clinical practice and should not be mistaken for intralabyrinthine metastases.
- Leigh Syndrome with Atypical Cerebellar LesionsPublication . Veiga, M; Marecos, C; Duarte, S; Vieira, JPLeigh Syndrome is a neurodegenerative disorder caused by mitochondrial dysfunction, with significant phenotypic and genetic heterogeneity. It usually presents in early life, with a severe prognosis. It can be caused by more than 75 different gene mutations, of nuclear and mitochondrial origin, involving all respiratory chain complexes, with less than 25% of Leigh syndrome having mitochondrial DNA mutations. The typical pathologic hallmarks are focal, bilateral, and symmetric lesions in the basal ganglia, thalamus, cerebellum, cerebral white matter and spinal cord gray matter, usually with T2WI and FLAIR hyperintensity. The basal ganglia and thalami frequently present with a pattern of cytotoxic edema. We present one case with clinical and analytical features consistent with Leigh Syndrome, with peculiar imaging features, showing dominant cerebellar edematous changes with unexpected petechial component suggestive of microangiopathy. To our knowledge, these features are unreported and suggest the existence of microvascular lesions. Based on the reported imaging findings, we propose that Leigh Syndrome should be added to the differential diagnosis of acute cerebellitis.
- Leigh Syndrome with Atypical Cerebellum Imaging FeaturesPublication . Veiga, M; Marecos, C; Vieira, JP; Conceição, C
- Periodontoid Pseudotumor in Tuberous Sclerosis Associated With Neck Diffuse LipomatosisPublication . Pinto, E; Veiga, M; Sagarribay, A; Conceição, CTuberous sclerosis (TS) is a genetic multisystem disorder associated with the development of benign tumors in many organs. Diffuse lipomatosis, which represents the overgrowth of fatty tissue in one part of the body, is a very rare finding reported in patients with tuberous sclerosis. We describe the case of a patient with diffuse lipomatosis in the right scapular, posterior cervical and perivertebral regions, associated with a space-occupying lesion adjacent to the odontoid process of C2 that appeared to be a pseudotumor, and discuss possible relation between these entities.