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1.
Skinmed ; 21(3): 187-189, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37634103

RESUMO

A 13-year-old Hispanic boy with no significant medical etymology presented with a chief complaint of widespread brown macules and patches. He had a large and evenly pigmented brown patch, with a centrally located 2.2 cm × 1.2 cm soft and darkly pigmented plaque, which became more apparent with tension applied to the surrounding skin (Figure 1). The patient's mother stated that the plaque was present since birth and had increased in size over time. The clinical differential diagnoses included a congenital melanocytic nevus (CMN), a large café au lait macule (CALM), and a Becker's nevus with a congenital smooth muscle hamartoma.


Assuntos
Hamartoma , Neurofibroma Plexiforme , Nevo Pigmentado , Masculino , Humanos , Adolescente , Neurofibroma Plexiforme/diagnóstico , Pele , Manchas Café com Leite , Nevo Pigmentado/diagnóstico
2.
Radiol Case Rep ; 13(4): 862-866, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-30174770

RESUMO

Tuberculous peritonitis is an uncommon extrapulmonary form of Mycobacterium tuberculosis infection, frequently presenting with nonspecific and insidious symptoms. Diagnosis is therefore difficult, unsuspected, and often delayed, especially in the pediatric patient without an obvious history of exposure to the pathogen. This report presents a 9-year-old Hispanic girl and a 3-year-old African American boy presenting with nonspecific and insidious symptoms, such as abdominal pain, distention, and fever in whom computed tomography findings of peritoneal thickening and enhancement, high density ascites, lymphadenopathy, and bowel wall thickening acted as key components in establishing a final diagnosis of the condition. Computed tomography is an important clinical adjuvant in making this difficult diagnosis.

3.
J Clin Imaging Sci ; 2: 78, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23393634

RESUMO

Congenital anomalous bands at the proximal jejunum resulting in obstruction have been described sporadically in the literature and are otherwise rare. We present a case of an 8 year-old girl with a nine-month history of intermittent vomiting and no history of prior surgery. The imaging workup includes an abdominal ultrasound, a single contrast upper gastrointestinal series, and a dual contrast computed tomography of the abdomen and pelvis. Surgical intervention revealed the presence of dense bands at the proximal jejunum without evidence of malrotation. Our report reviews the embryology and radiologic findings of this entity using different imaging modalities.

4.
Case Rep Radiol ; 2012: 151020, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22844628

RESUMO

Early diagnosis of ovarian torsion is critical in avoiding complications and planning management. Therefore, it is important to understand and assess the imaging findings of ovarian torsion. Ultrasound is the imaging modality of choice; however, it is not always definitive and diagnosis can be challenging. MRI is a better imaging modality to evaluate for signs of complications and to arrive at a more definitive diagnosis. We present a case of in utero ovarian torsion diagnosed during routine prenatal ultrasound with imaging findings on ultrasound and MRI postnatally.

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