Case report
Isolated right adrenal metastasis from an invasive
ductal breast
carcinoma.
Taha Mohammed Hassan 1*, Al Emadi Mohammed Abdullah 1, Lotfy Mohammed
1, Mustafa Mohamed Naser 2, Omar Amany Mohammed
Rabie 3, El
Mahdi Hoda Saleh 3.
1: Department
of
surgery 2: Department of radiology 3: Department
of pathology Al Emadi Hospital Doha, Qatar. *Corresponding author Correspondence to: Dr.taha@alemadihospital.com.qa Publication data: Submitted: April 23,2019 Accepted: June 27,2019 Online: October 15,2019 This article was subject to full
peer-review. This art This is an open access article distributed under the terms of the Creative Commons Attribution Non- Commercial License 4.0 (CCBY-NC) allowing to share and
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Introduction Invasive ductal carcinoma (IDC) is the most
common histopathological type of breast cancer,
accounting for up to 85% of all invasive breast carcinomas [1]. It spreads usually to the bone first.
Solitary metastasis is commonly located in the lung, liver or brain
[2]. Adrenal
glands locations are extremely rare [3]. We report
a case of isolated metachronous right adrenal metastasis, diagnosed
four years after breast IDC management. The aim is to highlight clinical, diagnostic and therapeutic characteristics of this entity. Case presentation We report
a case of 53 years old female
referred to surgery for right adrenal mass.
On her history
we noted a previous tumorectomy
followed by chemo and radiotherapy
for right breast invasive ductal carcinoma moderately differentiated Not Otherwise Specified (IDC-NOS). The
TNM staging of the tumor was T2 NX M0. On the four-year follow-up consultation, an incidental right suprarenal tumor was detected by abdominal ultrasound. CT and MRI scan
(Figure 1), confirmed the presence of a 5x7
cm right adrenal
gland mass.
Endocrinological workup revealed that the tumor was not secreting. The patient underwent Laparoscopic Adrenalectomy which had to be converted to open, from which the patient made uneventful recovery. Gross examination revealed firm capsulated
right adrenal mass, measuring 9 x 7 x 3 cm and about 123.5 grams
in weight with cut sections showed heterogenous cystic appearance. Microscopic examination revealed infiltration by sheets, clusters and cords of malignant cells
(figure 2a) with enlarged nuclei,
prominent nucleoli and frequent mitosis. The tumor
reached the surrounding fat with
focal vascular invasion (figure 2b).Immunohistochemical staining revealed that tumor
cells expressed diffuse positive staining with ER (2+ in 80% of tumor cells)
(figure 4a), PR (2+ in 2% of tumor
cells), GATA3
(figure 4b), E-cadherin, BCL-2, HER-2 is equivocal (2+) and Ki67 proliferation index was 30%.
Histopathological confrontation of both
adrenal and breast
specimens revealed identical morphological and immunohistochemical features and was consistent with metastatic mammary carcinoma. Thereafter, the patient received
6 cycles of chemotherapy followed by hormonal therapy and kept a regular follow up until
now. |
a b c
Figure1: Imaging features of the right incidentaloma.
(a) CT scan
showed 5x7x4 heterogenous mass of the right suprarenal region. (b,c) right
adrenal origin confirmed by MRI out phases
showed a well-defined
tumor arising from the adrenal
gland with mass effect
behavior on the right kidney
a b
C d
Figure 2: pathological examination
(a)Histology section shows adrenal tissue infiltrated by sheets of malignant cells (H and E, x200). (b) Histology
section shows vascular invasion (H and E, x200). (c) Diffuse
positive nuclear staining for ER (ER immunostaining, x200). (d) Diffuse positive nuclear staining for GATA3 (GATA3 immunostaining, x400).
The first published case of breast metastasis at adrenal gland was by Liu et al in 2010 [1]. Only eight cases of adrenal metastases from invasive breast carcinoma not otherwise specified were published up to date [2]. In six cases the metastasis was to the left adrenal gland [1,2] and in only two cases metastasis was to the right adrenal gland [3] as our case. We have reported an incidental right adrenal metastasis which originated from moderately differentiated invasive ductal carcinoma managed four year before. Adrenal metastatic tumors are often misdiagnosed as primary adrenal tumors. CT scan and MRI are suitable methods for distinguishing between a metastatic and primary adrenal tumor [4,5]. Additionally, immunoassaying of tissue sections can confirm the primary site [6]. In our case immunoassaying confirmed the breast origin. Patients with adrenal metastasis usually are asymptomatic and start to express suprarenal gland disfunction only when most of the adrenal gland is replaced or destroyed [7,8]. Our patient underwent Laparoscopic Right Adrenalectomy which was converted to open due to the large size of the tumor. In eight published cases, one case was treated by Lapatinib® [9] and the remaining cases was treated by open or laparoscopic Adrenalectomy [9]. The ideal treatment options of this condition are still unclear because of the rarity of solitary adrenal metastases from mammary carcinoma. Metastatic breast cancer is often fatal and the treatment in most of the cases is mainly limited to palliation chemotherapy or hormonal treatment. However, laparoscopic adrenalectomy for solitary adrenal metastasis is considered convenient, and could lead to a longer survival in some patients [10,11]. Even though it is important to avoid port-site metastasis and carcinomatosis which may happen after the procedure. Laparoscopic adrenalectomy is widely applied to adrenal gland tumors. However, the gold standardization in adrenal cancer metastasis remains controversial [12].
Although adrenal metastasis of an IDC is very rare, the present case is the ninth reported breast cancer metastatic to the adrenal gland. Definite diagnosis can be established by CT, MRI and histopathological examination. Early recognition and complete adrenalectomy may lead to survival benefit.
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Citation: Taha MH, Al Emadi MA, Lotfy M,
Mustafa MN, Omar A, El Mahdi H. Isolated right adrenal metastasis from
an invasive ductal
breast carcinoma. Junior medical
research.2019;2(2): 10-13. Taha
et al © All rights are reserved.
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