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AJR 2000; 174:1060
© American Roentgen Ray Society


Radiologic-Pathologic Conferences
of Wake Forest University Baptist Medical Center

Angiofollicular Lymphoid Hyperplasia (Castleman Disease) of the Axilla

Liem T. Bui-Mansfield1, Felix S. Chew1 and Cris P. Myers2

1 Department of Radiology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157-1088
2 Department of Pathology, Walter Reed Army Medical Center, 6900 Georgia Ave. N. W., Washington, DC 20307.



 
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 F. S. Chew.


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Introduction
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A 37-year-old woman presented with a left axillary mass, suggestive of a lymph node metastasis from a primary malignancy in the breast. Although bilateral mammography showed a homogeneously dense axillary mass, no primary lesion was detected. Sonography of the axilla showed an ovoid hypoechoic 3-cm (maximum diameter) mass (Fig. 1A). The lesion contained hypoechoic tubular structures with blood flow shown on color Doppler sonography (Fig. 1B). Excisional biopsy was performed. Microscopic sections of the enlarged lymph node showed numerous small folliclelike structures with radially penetrating capillaries, some with hyalinization in the central portion. A prominent vascular proliferation filled the perifollicular tissue (Fig. 1C). A perifollicular concentric layering of small lymphocytes ("onion skinning") was noted on high-power magnification (Fig. 1D). The final pathologic diagnosis was angiofollicular lymphoid hyperplasia, hyaline vascular type (Castleman disease).



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Fig. 1A. —37-year-old woman with angiofollicular lymphoid hyperplasia of axilla. Sonogram of axilla shows ovoid hypoechoic mass containing hypoechoic tubular structures.

 


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Fig. 1B. —37-year-old woman with angiofollicular lymphoid hyperplasia of axilla. Color Doppler sonogram shows vascular flow within mass.

 


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Fig. 1C. —37-year-old woman with angiofollicular lymphoid hyperplasia of axilla. Photomicrograph of histopathologic specimen shows lymphoid follicles surrounded by stroma that contain numerous hyperplastic capillaries, venules, and arterioles. (H and E, low power)

 


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Fig. 1D. —37-year-old woman with angiofollicular lymphoid hyperplasia of axilla. Photomicrograph of histopathologic specimen shows concentric layering of follicular lymphocytes around hyalinized central vessel producing characteristic "onion skin" pattern. (H and E, high power)

 

Angiofollicular lymphoid hyperplasia is an unusual inflammatory condition of unknown cause. It may be localized or generalized. Eighty-six percent of lesions are found in the mediastinum or hilum, and 91% are of the hyaline vascular type [1]. Histologically, hyaline vascular angiofollicular lymphoid hyperplasia is characterized by multiple germinal centers separated by a polymorphous lymphoreticular infiltrate containing numerous capillaries. It is usually asymptomatic. Less common is a plasma cell type with fewer capillaries and numerous plasma cells between the germinal centers. This variant often produces systemic manifestations, including fever, anemia, weight loss, and hypergammaglobulinemia. The prominent vascular proliferation characteristic of angiofollicular lymphoid hyperplasia is not seen in healthy or reactive lymph nodes and is also absent from lymph nodes involved with malignancy. The vascular pattern present in hyaline vascular angiofollicular lymphoid hyperplasia, when shown on color Doppler sonography, may help suggest the specific diagnosis and help differentiate this benign process from nodal metastases.

On CT, hyaline vascular angiofollicular lymphoid hyperplasia would appear as a homogeneous mass with marked contrast enhancement. Angiography would show a prominent tumor blush. MR imaging would show homogeneous architecture with hypointensity on T1-weighted images and hyperintensity on T2-weighted images. Sonography would show a hypoechoic mass with hyperechoic regions [2], and color Doppler sonography would show an artery penetrating the hilum of the mass and fine accessory peripheral arteries [3].

The differential diagnosis of an axillary mass in a woman includes metastases; lymphoid neoplasms; and a number of reactive, inflamamtory, and benign conditions. A homogeneously dense axillary mass evident on mammography has a significant probability of being metastatic breast cancer, and fine-needle aspiration or excisional biopsy of the mass should be considered to establish a definitive diagnosis [4].


References
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Introduction
References
 

  1. Keller AR, Hochholzer L, Castleman B. Hyalinevascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations. Cancer 1972;29: 670 -683[Medline]
  2. Yamashita Y, Hirai T, Matsukawa T, Ogata I, Takahashi M. Radiological presentations of Castleman's disease. Comput Med Imaging Graph 1993;17: 107 -117[Medline]
  3. Konno K, Ishida H, Hamashima Y, Komatsuda T, Matsamune O. Color Doppler findings in Castleman's disease of the mesentery. J Clin Ultrasound 1998;26: 474 -478[Medline]
  4. Walsh R, Kornguth PJ, Soo MS, Bentley R, DeLong DM. Axillary lymph nodes: mammographic, pathologic, and clinical correlation. AJR 1997;168: 33 -38[Abstract/Free Full Text]

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