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AJR 2002; 179:790
© American Roentgen Ray Society


Radiologic—Pathologic Conference of Keller Army Community Hospital at West Point, the United States Military Academy: Bilateral Temporal Fossa Hemangiomas

Liem T. Bui-Mansfield1,2,3, Cris P. Myers4, Douglas Fellows1 and Glen Mesaros5

1 Department of Radiology, Keller Army Community Hospital, 900 Washington Rd., West Point, NY 10996-1197.
2 Department of Radiology, Uniformed Services University of Health Sciences 4301 Jones Bridge Rd., Bethesda, MD 20814-4799.
3 Department of Radiology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157-1088.
4 Department of Pathology, Walter Reed Army Medical Center, 6900 Georgia Ave., Washington, DC 20307-5001.
5 Department of Surgery, Keller Army Community Hospital, West Point, NY 10996-1197.

Received February 8, 2002; accepted after revision March 4, 2002.

 
The opinions and assertions contained herein are those of the authors and should not be construed as official or as representing the opinions of the Department of the Army or the Department of Defense.

Address correspondence to L. T. Bui-Mansfield.


Introduction
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Introduction
References
 
A 44-year-old man presented with a right temporal fossa mass. Preoperative CT revealed heterogeneously enhancing, well-circumscribed, soft-tissue masses in both temporal fossae. On T1-weighted MR images, the masses were isointense relative to muscle. On T2-weighted MR images, the masses had predominantly heterogeneous high signal intensity with foci of low signal intensity (Fig. 1A). After gadolinium administration, patchy enhancement was present (Fig. 1B). The patient underwent excision of both masses (Fig. 1C). Histologic evaluation of these masses was consistent with cavernous hemangiomas (Fig. 1D).



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Fig. 1A. Bilateral temporal fossa hemangiomas in 44-year-old man. Axial T2-weighted MR image shows well-circumscribed high-signal masses with central low-signal-intensity dots (arrowheads) in both temporal fossae.

 


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Fig. 1B. Bilateral temporal fossa hemangiomas in 44-year-old man. Coronal T1-weighted MR image with fat suppression and gadolinium administration shows patchy enhancement of masses (arrowheads).

 


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Fig. 1C. Bilateral temporal fossa hemangiomas in 44-year-old man. Intraoperative photograph shows lobulated vascular mass (arrow) in right temporal fossa.

 


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Fig. 1D. Bilateral temporal fossa hemangiomas in 44-year-old man. Photomicrograph of pathology specimen shows well-circumscribed proliferation of large, thin-walled, dilated blood-filled vessels arranged in diffuse haphazard pattern. Walls of these vessels consist predominantly of dense fibrous connective tissue lined by flattened endothelium. (H and E,x4)

 

Soft-tissue masses of the temporal fossa are rare. Differential diagnoses include epidermoid cyst, soft-tissue sarcoma, metastasis, myositis ossificans, temporal arteritis, arteriovenous malformations, and temporal muscle herniation through a defect of the anterior temporalis fascia.

Hemangioma is one of the most common soft-tissue tumors, constituting 7% of all benign tumors. Hemangioma is a benign vascular lesion that may contain nonvascular elements such as fat, fibrous and myxoid tissue, smooth muscle, thrombus, and even bone. Hemangiomas are classified histologically by the predominant type of vascular channel (capillary, cavernous, arteriovenous, or venous) [1]. Fourteen percent of hemangiomas are found in the head and neck, occurring in the masseter, trapezius, and sternocleidomastoid muscles. Hemangioma of the temporal fossa is rare, usually involving the temporal muscle [2].

On radiography, hemangiomas appear as non-specific soft-tissue masses. Phleboliths are seen in 30% of the hemangiomas, most frequently in cavernous hemangiomas [1]. CT reveals a soft-tissue mass with associated fat overgrowth and serpentine vascular components, which may enhance after administration of contrast material. Sonography shows a complex mass with high-vessel density (> five vessels per square centimeter) and a peak arterial Doppler shift exceeding 2 kHz (sensitivity, 84%; specificity, 98%) [3]. MR imaging is considered the best modality for evaluating hemangiomas. Characteristic MR imaging features include lobulation, septation, central low-signal-intensity dots, and marked enhancement after gadolinium administration [4]. The septate—lobulated appearance of hemangiomas revealed on T2-weighted images correlates with fibrous and fatty septa (low signal intensity) between endothelial-lined vascular channels (high signal intensity). The central lowsignal-intensity dot sign seen on T2-weighted imaging may represent fibrofatty septa seen in cross section, hyalinized or thrombosed vascular channels, smooth muscle components, fast flow in blood vessels, calcification, or ossification.

Many forms of therapy have been used to control or cure hemangiomas: steroids, radiation, sclerosing agents, interferon alfa-2a, pentoxifylline, and surgical excision.


References
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Introduction
References
 

  1. Murphey MD, Fairbairn KJ, Parman LM, Baxter KG, Parsa MB, Smith WS. Musculoskeletal angiomatous lesions: radiologic-pathologic correlation. RadioGraphics 1995;15:893 -917[Abstract]
  2. Murakami M, Nonaka N, Hirata Y, Sonoda H, Ushio Y. Hemangioma of the temporalis muscle: case report and review of the literature. Surg Neurol 1991;36:388 -393[Medline]
  3. Dubois J, Patriquin HB, Garel L, et al. Soft-tissue hemangiomas in infants and children: diagnosis using Doppler sonography. AJR 1998;171:247 -252[Abstract/Free Full Text]
  4. Teo ELHJ, Strouse PJ, Hernandez RJ. MR imaging differentiation of soft-tissue hemangiomas from malignant soft-tissue masses. AJR 2000;174:1623 -1628[Abstract/Free Full Text]

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