2014, Number 5
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Rev Invest Clin 2014; 66 (5)
Idiopathic granulomatous mastitis. Experience at a cancer center
Cornejo-Juárez P, Vilar-Compte D, Pérez-Jiménez C, González-Ordoñez H, Maldonado-Martínez H, Pérez-Badillo MP, Villaseñor-Navarro Y, Volkow-Fernández P
Language: English
References: 14
Page: 393-398
PDF size: 381.55 Kb.
ABSTRACT
Background. Idiopathic granulomatous mastitis (IGM) is a
benign breast disease that has been described as a rare granulomatous
inflammation (GI). It can mimic inflammatory
breast cancer.
Material and methods. We included women
with a diagnosis of IGM referred to an oncologic hospital between
January 01, 2007 and to March 31, 2011, with diagnosis
of breast cancer, in whom biopsy reported GI, without other
cause related. The aim of this study was to review the clinical,
radiologic and pathologic characteristics of a cohort of women
with IGM.
Results. We analyzed 58 patients; mean age was
38 ± 12 years. Mammography showed diffuse asymmetry
(n = 19) and focal asymmetry (n = 13); breast ultrasound
showed heterogeneous and hypoechoic areas (n = 28) and
lumps (n = 21) as the most frequent lesions. All biopsies
showed lobulocentric GI. Treatment included antibiotics (n = 20),
steroids (n = 8), both treatments (n = 20), surgical excision
(n = 3) and observation (n = 7). Forty-three patients (74%)
had complete remission; mean time to remission was 9.5 ± 5.8
months. Fifteen (26%) had partial remission. Any patient had
progression or relapse.
Conclusions. IGM is a benign breast
condition that may mimic breast inflammatory cancer. Ultrasonography
and mammography findings reveal characteristic
data that can be useful for establishing the diagnosis; however,
biopsy is the gold standard for its diagnosis and should be
taken in any patient even with a mild suspicion of cancer.
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