July 30, 2009

Enchondroma of the Foot

Figure 1: AP radiograph of the left foot shows an incidental geographic lytic lesion without sclerotic border at the proximal phalanx of the third toe. There is cortical thinning without breakthrough or associated soft tissue mass. No matrix is visualized.
Figure 2: Sagittal MR image (STIR sequence) shows the lesion as markedly T2 hyperintense without associated soft tissue mass.


Facts
  • Enchondroma is common (10% of all benign bone tumors)
  • Most common in hands and feet
  • Occurs from cartilaginous cell nests displaced from physis during development
  • Often asymptomatic and found incidentally or after a pathologic fracture
  • Main differential diagnosis is chondrosarcoma, which is relatively rare in the foot - and typically arises de novo. However, differentiation using clinical and radiographic parameters can be difficult.
  • Presence of soft tissue mass, cortical destruction and deep endosteal scalloping - although suggests chondrosarcoma - can be seen in both benign and malignant cartilage tumors of the foot
When to Suspect Chondrosarcoma Arising from Enchondroma of the Foot?
  • Lesions larger than 5 cm
  • Midfoot or hindfoot
  • These lesions should be considered malignant and biopsy or close clinical follow up recommended

Reference:
Gajewski DA, Burnett JB, Murphy MD, Temple HT. Differentiating clinical and radiographic features of enchondroma and secondary chondrosarcoma in the foot. Foot Ankle Int 2006;27:240-242.

July 27, 2009

Fibromatosis Colli of Infancy

Transverse ultrasound images of the right sternocleidomastoic (SCM) muscle and left (symptomatic side) shows diffuse enlargement of the left SCM with mixed echogenicity in a 2-month-old infant.


Facts: Fibromatosis Colli of Infancy
  • Abnormal mass-like enlargement of sternocleidomastoic (SCM) muscle
  • Born normal but develops SCM mass and/or torticollis within the first 4-8 weeks of life
  • Associated with difficult delivery and intrauterine torticollis due to malposition
  • Histology: collagen fibers and fibroblasts around atrophied muscle fibers
  • Early diagnosis and treatment important because it can result in contracture
  • Responds well to physiotherapy
Ultrasound Appearance
  • US performed to exclude other diagnosis such as cervical lymphadenopathy, rhabdomyosarcoma, lymphoma, cystic hygroma or branchial cleft cyst
  • Mass or fusiform enlargement of the SCM muscle
  • Confined to muscle, no adjacent abnormalities of other soft tissues
  • Variable echogenicity -- hyperechoic, hypoechoic, or mixed echogenicity
Reference:
Bedi DG, John SD, Swischuk LE. Fibromatosis colli of infancy: variability of sonographic appearance. J Clin Ultrasound 1998;26:345-348.

July 24, 2009

Embryonic Demise

Figure 1: Transvaginal ultrasound shows a mean sac diameter of 30 mm (about 8 weeks gestational age). S = gestational sac.
Figure 2: Further scan demonstrates a fetal pole (arrow) without a yolk sac. There is minimal decidual reaction.


Embryonic Demise
  • Most common cause = chromosomal abnormality leading to arrested development
  • Diagnosis is made by:
  1. CRL > 5 mm but no cardiac activity
  2. MSD >/= 8 mm but no yolk sac
  3. MSD >/= 16 mm but no embryo
  4. Embryo seen but no yolk sac
  5. No cardiac activity in embryo seen by transabdominal ultrasound (need to confirm with transvaginal ultrasound if early IUP)

Reference:
Weissleder, Wittenberg, Harisinghani, Chen. Primer of diagnostic imaging. 4th edition, 2007

July 21, 2009

Unilateral Opacity of a Hemithorax

Figure 1: Supine chest radiograph shows a unilateral increased opacity in the left hemithorax, particularly at the mid to lower zones. There is no mediastinal shift. The left hemidiaphragm is in a normal position.


Differential Diagnosis
  1. Lung: consolidation, mass, collapse
  2. Pleura: effusion (layering or loculated), mass (metastasis, mesothelioma)
  3. Chest wall: mass (breast, chest wall musculatures)
  4. Extrathoracic: external structures

In this case, the opacity extends beyond the lung to the soft tissue of the chest wall, corresponding to the breast. It is unlikely to be a lung lesion because normal pulmonary vasculatures are visualized through it. Pleural lesion would not extend beyond the thoracic cage. Two main possibilities include a large breast mass or external structures (for example, nonradiopaque pads on the bed).

Comparison with the previous chest radiographs revealed that this is a new finding. Further query of patient's history confirmed the diagnosis of a large left breast mass. Chest CT scan (below) also shows the mass (invasive cancer).


Reference:
Chapman S and Nakielny R. Aids to radiological differential diagnosis. 4th edition, 2003.

July 18, 2009

Double Bubble Sign

Supine abdominal radiograph of a newborn presenting with billous vomiting shows a distended stomach and duodenal air bubbles "double bubble" sign. There is no gas distal to the duodenal bubble. Radiopaque materials overlying the right pelvis are due to soiled diaper.


Double Bubble Sign
  • Radiographic signs describing two air-filled structures in the upper abdomen with little or no air distally
  • Can be reproduced in upper GI study or ultrasound
  • Left-sided bubble = stomach
  • Right-sided bubble (usually right of midline) = duodenum
  • Most common cause = duodenal atresia
Differential Diagnoses
  • Intrinsic cause: duodenal atresia, duodenal stenosis, duodenal web
  • Extrinsic cause: annular pancreas, malrotation with obstruction produced by midgut volvulus or by Ladd bands
Main Concern
  • Must be differentiated from 'malrotation with obstruction (midgut volvulus)' because this condition requires urgent surgery
  • Suspect midgut volvulus if stomach is distended but duodenum is normal or only slightly dilated

Reference:
Traubici J. The double bubble sign. Radiology 2001;220:463-464.

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