J Korean Soc Magn Reson Med.  2010 Jun;14(1):74-77. 10.13104/jksmrm.2010.14.1.74.

Sino-orbital Granulocytic Sarcoma Causing Bilateral Proptosis As an Initial Manifestation of Acute Myelogenous Leukemia (AML): A Case Report

Affiliations
  • 1Department of Radiology, Ansan Hospital, College of Medicine, Korea University, Korea. radje@korea.ac.kr

Abstract

Granulocytic sarcoma is a manifestation of myelogenous leukemia, which means a solid mass consisting of primitive precursors of the granulocytic series of white blood cells. We present CT and MR imaging findings of bilateral sino-orbital granulocytic sarcoma in a 22-month-old boy. The mass involved bilateral orbital fossa which resulted in bilateral proptosis. Moreover, the mass extended to the almost skull base including paranasal sinuses, maxilla, temporal bone, zygomatic bone, sphenoid bone, ethmoid, and palatine bone. The adjacent dura was continuously thickened and the lower half of cavernous sinus was also involved. The patient was diagnosed as AML (M5) with t(8,21) translocation through a chromosome study from the bone marrow.

Keyword

Leukemia; Myeloid; Acute; Granulocytic sarcoma; Orbital neoplasms

MeSH Terms

Bone Marrow
Cavernous Sinus
Ethmoid Bone
Exophthalmos
Humans
Infant
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukocytes
Maxilla
Orbit
Orbital Neoplasms
Palate, Hard
Paranasal Sinuses
Sarcoma, Myeloid
Skull Base
Sphenoid Bone
Temporal Bone

Figure

  • Fig. 1 Orbital CT in a 22-month-old boy with bilateral proptosis. (Left) Non-enhanced coronal reformatted CT in a soft tissue window setting demonstrated hyperdense masses in bilateral inferolateral walls of orbits, PNS, maxillae and temporal regions. (Right) Coronal reformatted CT in a bone window setting presented expansion of medullary cavity of frontal bone, maxilla and zygoma and no destruction of bony cortex. Most of skull base including temporal, sphenoid, palatine and ethmoid bones was also involved (not shown).

  • Fig. 2 Contrast-enhanced orbital MR in the same patient. T1-weighted (Left upper) and T2-weighted (Right upper) axial images at the level of optic nerve showed iso-intense masses surrounding the bilateral lesser wings of sphenoid bone. On contrast-enhanced T1-weighted axial image (Left lower), the masses were homogeneously and strongly enhanced. Coronal image (Right lower) at the maxillary infundibular level presented homogeneous and strong enhancement in the bilateral peri-orbital soft tissue, temporal bone, maxilla, zygoma and surrounding soft tissue.


Reference

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