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AJR 2002; 178:1236-1238
© American Roentgen Ray Society


Case Report

Aspergilloma of the Breast in a Woman with Acute Myeloid Leukemia

Stephan P. Kloska1, Karl Ludwig1, Michael Kreuter2, Raihanatou Diallo3 and Walter Heindel1

1 Department of Clinical Radiology, University of Muenster, Albert-Schweitzer-Str. 33, 48149 Muenster, Germany.
2 Department of Medicine/Hematology and Oncology, University of Muenster, 48149 Muenster, Germany.
3 Gerhard-Domagk-Institute of Pathology, University of Muenster, Domagkstr. 17, 48149 Muenster, Germany.

Received July 30, 2001; accepted after revision October 10, 2001.

 
Address correspondence to S. P. Kloska.


Introduction
Top
Introduction
Case Report
Discussion
References
 
Invasive aspergillosis is a common opportunistic infection in immunocompromised patients [1,2,3]. It usually affects the pulmonary system. Extrapulmonary manifestations are rare. Invasive aspergillosis has been described in the brain, skin, heart, kidney, and gastrointestinal tract [4, 5].

This report presents a finding of invasive aspergilloma of the breast in a patient with acute myeloid leukemia. Histologic findings and corresponding radiologic features in mammography and sonography are described.


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 40-year-old woman presented with a newly developed lump in the right breast. She had a history of acute myeloid leukemia diagnosed 2 years previously, with complete remission after chemotherapy. A relapse 1 year after initial diagnosis had been treated by allogeneic stem cell transplantation. A graft-versus-host disease of the skin and the intestine developed on day 17 after transplantation and was treated with high doses of corticosteroids and cyclosporin A. Eight weeks later, still immunosuppressed, she had developed pneumonia with a consolidating infiltrate of the right lower lobe. Microbiology findings revealed aspergillus flavus in the specimen of a bronchoalveolar lavage. Therefore, the patient received antimycotic therapy with voriconazole (Vfend; Pfizer, New York, NY). Three months after stem cell transplantation, she detected a newly developed breast lump in the right upper lateral quadrant.

On physical examination, the lump was superficially located in the right upper lateral quadrant. It was mobile against the surrounding tissue and had a moderate resistance. The skin of the breast showed no signs of inflammation. Three small cutaneous nodes were palpable in the right infraclavicular region, as was one lesion at the right upper arm, none of which had been noted by the patient.

Mammography revealed an inhomogeneous opaque lesion in the right upper lateral quadrant (Figs. 1A and 1B) that had a lobulated shape and an ill-defined border to the surrounding tissue without a halo sign. No calcification was seen in the lesion.



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Fig. 1A. 40-year-old woman with newly developed lump in right breast in underlying acute myeloid leukemia. Craniocaudal (A) and oblique (B) mammograms show inhomogeneous opaque lesion in right upper lateral quadrant. Lobulated shape and ill-defined border to surrounding tissue can be seen. No calcification and no halo sign are evident.

 


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Fig. 1B. 40-year-old woman with newly developed lump in right breast in underlying acute myeloid leukemia. Craniocaudal (A) and oblique (B) mammograms show inhomogeneous opaque lesion in right upper lateral quadrant. Lobulated shape and ill-defined border to surrounding tissue can be seen. No calcification and no halo sign are evident.

 

Sonography showed a lesion with a thin, distinct hypoechogenic border, a moderate hypoechogenic center, and mild, irregular acoustic shadowing. The lesion was 2 x 1.6 x 0.9 cm (Fig. 1C).



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Fig. 1C. 40-year-old woman with newly developed lump in right breast in underlying acute myeloid leukemia. Sonogram of right upper lateral quadrant, obtained at 7.5 MHz, shows lesion (markers) with thin, well-defined hypoechogenic border, moderately hypoechogenic center, and mild, irregular acoustic shadowing.

 

Because the patient had undergone mammography 4 months earlier with unremarkable findings, carcinoma of the breast seemed unlikely. Our main differential diagnosis was the rare leukemic infiltration of the breast tissue known as granulocytic sarcoma [6].

A biopsy of the breast lesion performed because of the unspecific radiologic findings revealed an extrapulmonary infiltration of aspergillus flavus. The small skin lesions proved to be extrapulmonary manifestations of aspergillosis as well.

Pulmonary aspergillosis proceeded despite antimycotic therapy; therefore, the patient underwent surgery with resection of the right lower lobe as well as the extrapulmonary lesions. A thin-walled, centrally necrotic lesion with a size of 2 x 1.7 x 1.2 cm was found in the resected breast tissue (Fig. 1D). Histologic examination showed this lesion to be a central abscess with a rim of organizing granulation tissue. A high-power view of the specimen revealed multiple branching hyphae with the typical appearance of aspergillus (Figs. 1E and 1F).



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Fig. 1D. 40-year-old woman with newly developed lump in right breast in underlying acute myeloid leukemia. Photograph of gross specimen that is 2 x 1.7 x 1.2 cm shows paracentrally located yellow—green necrotic area.

 


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Fig. 1E. 40-year-old woman with newly developed lump in right breast in underlying acute myeloid leukemia. Photomicrograph of histologic section reveals mammary abscess with surrounding inflammatory infiltrate and some breast ducts (arrow). (H and E, x25)

 


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Fig. 1F. 40-year-old woman with newly developed lump in right breast in underlying acute myeloid leukemia. High-power photomicrograph of histologic section shows multiple branching hyphae with typical appearance of aspergillus. (H and E, x400)

 


Discussion
Top
Introduction
Case Report
Discussion
References
 
In an indolent, growing breast lump without signs of inflammation, primary carcinoma of the breast is the most likely diagnosis. Metastases to the breast from an extramammary tumor are rare [7]. The mammographic appearance of the mass in our patient contained both soft tissue and fat elements. Therefore, hamartoma would have been another differential diagnosis, had it appeared on the previous mammograms.

In patients with an underlying hematologic malignancy, granulocytic sarcoma (chloroma) has been reported as a rare breast tumor [6]. Granulocytic carcinoma is an extramedullary tissue mass of blasts and immature myeloid cells. The surface of a freshly cut of granulocytic carcinoma turns light green (hence the name chloroma) upon exposure to air, when large amounts of peroxidase are oxidized. Granulocytic sarcoma may represent the initial manifestation of acute leukemia or signal relapse. The mammographic and sonographic findings in our patient were indistinguishable from those seen in carcinoma of the breast and granulocytic sarcoma.

Aspergillosis is an opportunistic infection having several risk factors affecting the immune system [2, 3, 8]. Aspergillus infection leads to hyphal growth and invasion of the blood vessels, hemorrhagic necrosis, infarction, and potential dissemination to any other organ in susceptible patients. It most commonly affects the lungs and paranasal sinuses; less frequently, extrapulmonary sites such as the brain, skin, gastrointestinal tract, heart, or kindney are involved [4, 5]. In our patient, risk factors for opportunistic infections were chemotherapy-induced granulocytopenia and the treatment with high doses of cyclosporin A and corticosteroids for graft-versus-host disease [8]. In some rare cases, aspergillus colonization of the breast tissue associated with silicone mammary implants has been reported [9]; those patients had no clinical evidence of infection or inflammation and were not immunosuppressed. Because of the unspecific radiographic findings in our patient, only biopsy could reveal the diagnosis.

Extrapulmonary aspergilloma has to be considered as a rare differential diagnosis in a newly developed breast tumor in immunocompromised patients, especially in patients with known pulmonary aspergillosis.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Walsh TJ, Pizzo PA. Nosocomial fungal infections: a classification for hospital-acquired fungal infections and mycoses arising from endogenous flora or reactivation. Annu Rev Microbiol 1988;42:517 -545[Medline]
  2. Jimenez C, Capdevila JA, Hidalgo A. Invasive pulmonary aspergillosis in a patient with acute myeloid leukemia. Haematologica 1999;84:1150 -1151[Medline]
  3. Khoo SH, Denning DW. Invasive aspergillosis in patients with AIDS. Clin Infect Dis 1994;19[suppl 1]:S41 -S48
  4. D'Antonio D, Pagano L, Girmenia C, et al. Cutaneous aspergillosis in patients with haematological malignancies. Eur J Clin Microbiol Infect Dis 2000;19:362 -365[Medline]
  5. Henochowicz S, Mustafa M, Lawrinson WE, Pistole M, Lindsay J Jr. Cardiac aspergillosis in acquired immunodeficiency syndrome. Am J Cardiol 1985;55:1239 -1240[Medline]
  6. Hiorns MP, Murfitt J. Granulocytic sarcoma (chloroma) of the breast: sonographic findings. AJR 1997;169:1639 -1640[Medline]
  7. Paulus DD, Libshitz HI. Metastasis to the breast. Radiol Clin North Am 1982;20:561 -568[Medline]
  8. Berenguer J, Allende MC, Lee JW, et al. Pathogenesis of pulmonary aspergillosis: granulocytopenia versus cyclosporine and methylprednisolone-induced immunosuppression. Am J Respir Crit Care Med 1995;152:1079 -1086[Abstract]
  9. Williams K, Walton RL, Bunkis J. Aspergillus colonization associated with bilateral silicone mammary implants. Plast Reconstr Surg 1983;71:260 -261[Medline]

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