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CASE REPORT
A rare case of tuberculous mastitis mimicking breast carcinoma
Richmond Ronald Gomes*
Department of Medicine, Ad-din Women’s Medical College and Hospital, Dhaka, Bangladesh
Received on: 13 June 2020; Revised on: 15 July 2020; Accepted on: 01 August 2020
ABSTRACT
There have been an increasing number of tuberculosis (TB) cases worldwide, but TB of the breast remains
rare. In rare cases, this is seen with a cutaneous manifestation of erythema nodosum. We report the case of
a 33-year-old woman with TB of the left breast accompanied by erythema nodosum on the anterior aspect
of both lower legs and dorsum of feet. Due to her poor clinical response to conventional therapy, and the
histopathological findings of fine-needle aspiration cytology with epithelioid granuloma with caseation,
there were strong indications of TB. She received antituberculous therapy (ATT) for 6 months. During
her follow-up examination after 6 months, no evidence of either residual or recurrent disease was present.
Histopathological features and a high index of clinical suspicion are necessary to confirm a diagnosis of
TB of the breast. ATT with or without simple surgical intervention is the core treatment.
Keywords: Antituberculous therapy, Caseation, Erythema nodosum, Granuloma, Tuberculosis
INTRODUCTION
Tuberculosis (TB) is one of the leading infectious
diseases worldwide. Extrapulmonary TB involving
the breast is extremely rare. It often mimics breast
carcinoma and pyogenic breast abscess clinically and
radiologically,maybothcoexist.Vulnerabilitytobreast
TB is increased in women who are young, married,
multiparous and who breastfeed.[1]
Histopathological
examination using fine-needle aspiration cytology
(FNAC) may reveal caseating epithelioid cell
granulomas and acid-fast bacilli (AFB).Although the
presence of an acid-fast stain or culture is essential
to confirm diagnosis, it does not give a positive
result in most patients.[2,3]
Molecular detection of
Mycobacterium tuberculosis by polymerase chain
reaction can be particularly useful in the validation
of a diagnosis of TB in clinical settings where the
diagnosis is uncertain.[3,4]
Diagnosis is usually based
on high index of suspicion, findings of granulomatous
lesion with Langhans’ giant cells, TB culture, and
response to antitubercular therapy (ATT). We report
a case of TB of the breast associated with a cutaneous
manifestation of erythema nodosum.
CASE REPORT
A 33-year-old married, recently detected diabetic
(on metformin), HIV-negative housewife
presented at medicine outpatient, Ad-din Women’s
Medical College and Hospital, Dhaka, with fever,
painful swelling over both shin and dorsum of the
feet, bilateral knee, and ankle pain for 8 days. She
also gave a history of gradually growing painful
discharging lump over her left breast for the past
1 month with on and off undocumented low-grade
fever. For the past 8 days, fever became high
grade, intermittent (maximum recorded 103°F)
associated with chills and rigor and subsided
temporarily after taking antipyretic. She did
not have any personal medical history of TB or
diabetes mellitus. She also neither had family
history of breast cancer nor had any contact history
with a patient with active TB. She also denied any
cough, weight loss, night sweat, anorexia, and
Available Online at www.ijms.co.in
Innovative Journal of Medical Sciences 2020; 4(3):1-5
ISSN 2581 – 4346
*Corresponding Author:
Dr. Richmond Ronald Gomes,
E-mail: rrichi.dmc.k56@gmail.com
Gomes: Tuberculous mastitis
IJMS/Jul-Sep-2020/Vol 4/Issue 3 2
bloody diarrhea. She was immunized as per EPI
schedule. With these complaints, she visited a
local physician and got 7 days second-generation
oral cephalosporin without any improvement. She
had a 3-year-old child.
On admission, she had a body temperature
of 102°F, blood pressure of 126/68 mmHg, a
pulse rate of 89/min, and a respiratory rate of
19/min. On physical examination, there was a firm,
erythematous, mass of 5 × 6 cm with brownish
discharge over the upper outer quadrant of her
left breast accompanied by retraction of adjacent
skin. Mass was not fixed to underlying structure or
overlying skin. Nipple, areola was normal. There
was also a firm, non-tender mobile lymph node
over left medial axilla. Dark reddish plaque skin
lesions were found over both lower legs and the
dorsal aspect of her feet. Both ankle and knee joints
were also red, swollen. There was also painful
restriction of both active and passive movement
in these joints. No other joints or axial skeleton
was involved. Her blood test results showed the
following: Hb% 9.3 gm/dl, MCV – 81, MCH
29,white blood cells at 15.20 × 103
/μL, neutrophils
at 77.3%, lymphocytes at 12.7%, platelets at 418 ×
103
/μL, C-reactive protein at 86.8 mg/dL (normal
range ≤5), and an erythrocyte sedimentation rate
during the 1st
h of 70 mm/h (normal ≤12). Peripheral
blood film revealed normocytic normochromic
anemia with neutrophilic leukocytosis. Her blood
culture revealed no growth, while her chest
radiography was unremarkable. MT was positive
with induration 14 mm after 72 h. ALT was 29 U/L,
serum calcium was 8.4 mg/dl, and random blood
sugar was 13.8 mmol/L.
An ultrasonography of our patient’s left breast
showed a lump measuring about 5 × 5 cm, which
was conglomerated, with an irregular margin
with hypoechoic heterogeneous echogenicity, and
with a left axillary lymph node. A core needle
aspiration biopsy of her left breast was also
performed. Under the microscope, this section
of her left breast showed chronic mastitis mixed
with granulation tissue and numerous foreign body
giant cells but with no evidence of malignancy
[Figure 1]. Background consisted of necrotic
material and fibrinous exudate. A culture of the
wound tissues failed to grow any organisms. Stains
for AFB were negative. Discharge for GeneXpert
Figure 1: Hematoxylin and eosin stain of our patients
breast tissue, showing giant cell (arrow) and inflammatory
cells
Figure 2: Healed ulcer with sinuses after 2 months of ATT
therapy
Figure 3: After 6 months of completion of ATT therapy
Gomes: Tuberculous mastitis
IJMS/Jul-Sep-2020/Vol 4/Issue 3 3
TB was not sent due to come unavoidable logistic
support. A dermatologist was consulted regarding
the dark reddish plaque skin lesions and treated
conservatively with NSAIDs.
Our final diagnosis tubercular mastitis was relied on
clinical suspicion, histopathological tissue findings,
and failure to respond to conventional antibiotic
therapy. She was put on a 6-month course of
antitubercular therapy with a 2-month intensive phase
ofrifampicin,isoniazid,ethambutol,andpyrazinamide
without steroid followed by a consolidation phase of
rifampicin and isoniazid for another 4 months. After
undergoing 4 months of antituberculous treatment,
her left breast mass and axillary node were gradually
reduced [Figure 2]. Although acid-fast stain showed
no tubercle bacilli, her ATT was continued. Her
left breast mass gradually became smaller and then
regressed. She was treated for 6 months without any
further complication [Figure 3]. She was regularly
followed up for another 6 months and no evidence of
the recurrence of her disease was noted.
DISCUSSION
TB remains one of the leading causes of death from
infectious diseases worldwide. Despite the fact that
it can affect any organ or site of the body, the breasts,
skeletal muscles, and spleen are the most resistant to
TB.[5,6]
TB comprises approximately 0.025%–0.1%
ofallsurgicallytreateddiseasesofthebreast,butthis
ratio is higher in underdeveloped countries.[7]
The
first description of mammary TB was given by Sir
Astley Cooper in 1829.[5]
He described TB mastitis
as “scrofulous swelling” in the bosom of young
women.Although breast TB is primarily considered
a disease of the developing world, a steady increase
in the incidence of the disease has also been seen in
developed countries. This is probably because of the
migration of the infected population from endemic
zones and an increasing number of patients who
are immunocompromised.[8]
Tuberculous mastitis
is more commonly seen in females of reproductive
age group, however, especially during the lactation
period, when they are more susceptible since the
lactating breast is more vascular and predisposed to
trauma.[4,5]
Both breasts are reported to be involved
with equal frequency. Bilateral disease is rare,
occurring in 3% of patients.[5]
The duration of symptoms varies from a few
months to several years, but in most instances, it
is less than a year. Constitutional symptoms such
as fever, weight loss, night sweats, or a failing of
general health are infrequently encountered[2]
and
are present 20% of cases. Our patient presented
only a month history of breast lump without much
constitutional symptoms. Its clinical manifestations
are variable. Patients usually have a positive
tuberculin skin test[9]
so as our patient had.
ThecommonpresentationofbreastTBisalumpinthe
breast with or without ulceration, may associate with
the sinus. Other presentations are diffuse nodularity
andmultiplesinuses.Multiplelumpsarelesscommon.
Pain in the lump is present more frequently in breast
TB cases than in breast carcinomas but our patient had
painful breast lump. The involvement of the nipple
and the areola is rare inTB. Fixation of the skin, which
resembles a neoplastic lesion, may also be present but
nipple discharge is uncommon.[10]
Associated axillary
lymphadenopathyisfoundinsomepatients[1,3,11]
asour
patient had. Other uncommon presentations include;
a typical undermined tuberculous ulcer, purulent
discharge from the nipple or with a fluctuant swelling
which, if inadvertently incised, produces a discharging
ulcer.[5,12]
Both breasts can be affected equally but
bilateralinvolvementisveryuncommon.Althoughthe
upper outer quadrant seems to be the most frequently
involved site due to its proximity to the axillary
nodes, any area of the breast can be affected.[9]
Lung
lesions (active or healed) on radiographic examination
are rare now. Mammography is of limited use since
the findings are often indistinguishable from a
malignancy[12]
and young patients have highly dense
breast tissue. Coexisting TB and carcinoma of the
breast were reported byAlzaraa et al.[13]
TB of the breast is mainly classified according
to its primary and secondary forms. Although
it was initially believed that as much as 60% of
breast TB was primary, it is now accepted that
mammary TB is almost invariably secondary to
a lesion elsewhere in the body. Primary infection
of the breast, however, through abrasions in the
skin or through the duct openings on the nipple is
a possibility. The most common mode of infection
is thought to be retrograde lymphatic spread from
the pulmonary focus through the paratracheal and
internal mammary lymph nodes. Hematogenous
Gomes: Tuberculous mastitis
IJMS/Jul-Sep-2020/Vol 4/Issue 3 4
spread and direct extension from contiguous
structures are other modes of infection.[5]
Breast TB was originally classified by McKeon
et al.[14]
into the following categories: (a) Acute
miliary type – rare, due to blood borne infection in
miliary TB; (b) nodular type – the most common
type, which presents as a localized lump with
or without sinuses in one quadrant of the breast;
(c) disseminated type – involving the entire
breast with multiple sinuses; (d) sclerosing type –
minimal caseation and extensive hyalinization of
the stroma, shrinkage of the breast tissue with early
skin retraction, and late sinus formation; clinically,
this type is indistinguishable from carcinoma;
and (e) tuberculous mastitis obliterans – a rare
form due to intraductal infection with fibrosis and
obliteration of the ductal system; sinus formation
is infrequent.[3,5,14]
Mantoux testing does not offer
definitive diagnosis, but confirms exposure of the
patient to tubercle bacilli.
Radiological imaging modalities such as
mammography and ultrasonography are unreliable
in distinguishing breast TB from breast carcinoma.
Similarly, computed tomography (CT) scan and
MRI do not give a conclusive diagnosis without
histopathological confirmation. CT scan is useful in
differentiating between the primary and secondary
forms.Itisalsohelpfulinevaluatingtherelationship
between deeply located lesions with the chest wall
and pleura and in detecting parenchymal lesions
of the lung. As such it provides valuable guides to
surgery and in defining the extent of the disease,
including the involvement of the chest wall.[11,15]
The demonstration of AFB from the lesions is
usually difficult.[16]
In tuberculous mastitis, AFB
are identified only in 12% of the patients. Our
patient also did not show any AFB in the lesion.
Therefore, clinical suspicion and demonstration
of caseating granulomas with Langhans’ giant
cells from the breast tissue and involved lymph
nodes may be sufficient for the diagnosis. In TB
endemic countries, the finding of granuloma in
FNAC warrants empirical treatment for TB even
in the absence of positive AFB and without culture
results.[16,17]
Detailed histological evaluation is,
however, mandatory to rule out a coexisting
carcinoma. Core needle aspiration biopsy from our
patients left breast revealed caseation, epithelioid
giant cells without any evidence of malignancy.
FNAC is very useful and it is a promising
technique in expert hands.[17]
Abiopsy is mandatory
for confirmation of diagnosis. Antituberculous
chemotherapy is still the main treatment for breast
TB, and no specific guidelines are available for this
kind of treatment. The disease should be treated
as any other form of extrapulmonary TB. ATT
comprises rifampicin, isoniazid, pyrazinamide,
and ethambutol for the initial 2 months, which
is then followed by rifampicin and isoniazid for
another 4 months. The extension of ATT from 12 to
18 months is required in patients with slow clinical
response, and complete resolution is obtained in
most patients. Our patient showed response in
6 months so further extension of therapy was not
given. FNAC should be repeated to confirm that
the residual mass is fibrotic. In refractory cases that
lead to breast destruction, a simple mastectomy may
be performed.[1,3,9,11]
Radical mastectomy is best
avoided unless there is a coexisting malignancy.[5,12]
The duration of follow-up after therapy is variable.
In a study by Shinde et al., all patients were
followed up for a minimum of 2 years to determine
that they were free of the disease after therapy.[1]
After complete ATT, residual lumps localized to a
quadrant should be excised through segmental or
sector mastectomy. Aspiration or surgical drainage
may be required in some cases.
The cutaneous involvement of TB is rare.
Underlying systemic involvement of TB is often
seen in cutaneous TB, especially in children.
Cutaneous TB is classified as true TB or
tuberculids. True cutaneous TB is composed of
tuberculous chancre, miliary TB, lupus vulgaris,
scrofuloderma, TB verrucosa cutis, tuberculous
metastatic abscess, and orificial TB. Tuberculids
are delayed sensitivity reactions to M. tuberculosis
in patients with a strong immune response.
Tuberculids include lichen scrofulosorum and
papulonecrotic tuberculid. Facultative tuberculids
consist of erythema induratum and erythema
nodosum. Erythema induratum is a recurrent,
painful subcutaneous nodule usually on the
posterior aspect of the leg. Biopsy shows lobular
panniculitis with vasculitis and granulomatous
inflammation. Erythema nodosum is a painful
subcutaneous nodule, mostly found on the anterior
Gomes: Tuberculous mastitis
IJMS/Jul-Sep-2020/Vol 4/Issue 3 5
aspect of the leg. Biopsy shows septal panniculitis
with an absence of vasculitis and usually without
granuloma. Erythema nodosum often occurs in
associationwithagranulomatousdisease,including
sarcoidosis, TB, and granulomatous colitis. TB
remains an important cause of erythema nodosum
in endemic countries.[18]
CONCLUSION
In endemic TB regions, a painful breast mass with
cutaneous manifestation of erythema nodosum
is clinically relevant to determine a diagnosis of
breast TB. To conclude, diagnosis of tuberculous
mastitis is usually based on high index of suspicion,
finding of granulomatous lesion with Langhans’
giant cells, and response to ATT. FNAC and biopsy
may also be inconclusive. AFB is not seen in most
cases. Prompt diagnosis and adequate treatment
can avoid unnecessary operation in these patients.
REFERENCES
1. Shinde SR, Chandawarkar RY, Deshmukh SP.
Tuberculosis of the breast masquerading as carcinoma:
A study of 100 patients. World J Surg 1995;19:379-81.
2. Akçay MN, Sağlam L, Polat P, Erdoğan F, Albayrak Y,
Povoski SP. Mammary tuberculosis--importance of
recognition and differentiation from that of a breast
malignancy: Report of three cases and review of the
literature. World J Surg Oncol 2007;5:67.
3. Tewari M, Shukla HS. Breast tuberculosis: Diagnosis,
clinical features and management. Indian J Med Res
2005;122:103-10.
4. Marchetti G, Gori A, Catozzi L, Vago L, Nebuloni M,
Rossi MC, et al. Evaluation of PCR in detection of
Mycobacterium tuberculosis from formalin-fixed,
paraffin-embedded tissues: Comparison of four
amplification assays. J Clin Microbiol 1998;36:1512-7.
5. Banerjee SN, Ananthakrishnan N, Mehta RB.
Tuberculous mastitis: A continuing problem. World J
Surg 1987;11:105-9.
6. Madhusudhan KS, Gamanagatti S. Primary breast
tuberculosis masquerading as carcinoma. Singapore
Med J 2008;49:e3-5.
7. Kalac N, Ozkan B, Bayiz H, Dursun AB, Demirag F.
Breast tuberculosis. Breast 2002;11:346-9.
8. Zandrino F, Monetti F, Gandolfo N. Primary tuberculosis
of the breast. A case report. Acta Radiol 2000;41:61-3.
9. Wilson JP, Chapman SW. Tuberculous mastitis. Chest
1990;98:1505-9.
10. Fadaei-Araghi M, Geranpayeh L, Irani S, Matloob R,
Kuraki S. Breast tuberculosis: Report of eight cases.
Arch Iran Med 2008;11:463-5.
11. Khanna R, Prasanna GV, Gupta P, Kumar M, Khanna S,
KhannaAK. Mammary tuberculosis: Report on 52 cases.
Postgrad Med J 2002;78:422-4.
12. Al Soub H, Chacko K. Tuberculous mastitis: A rare
disease. Br J Clin Pract 1996;50:50-1.
13. Alzaraa A, Dalal N. Coexistence of carcinoma and
tuberculosis in one breast.World J Surg Oncol 2008;6:29.
14. Mckeown KC, Wilkinson KW. Tuberculous disease of
the breast. Br J Surg 1952;39:420-9.
15. Kervancioğlu S, Kervancioğlu R, Ozkur A, Şirikçi A.
Primary tuberculosis of the breast. Diagn Interv Radiol
2005;11:210-2.
16. Kakkar S, Kapila K, Singh MK, Verma K. Tuberculosis
of the breast. A cytomorphologic study. Acta Cytol
2000;44:292-6.
17. Mehrotra R. Fine needle aspiration diagnosis of
tuberculous mastitis. Indian J Pathol Microbiol
2004;47:377-80.
18. Sethuraman G, Ramesh V, Raman M, Sharma VK. Skin
tuberculosis in children: Learning from India. Dermatol
Clin 2008;26:285-94.

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A rare case of tuberculous mastitis mimicking breast carcinoma

  • 1. © 2020, IJMS. All Rights Reserved 1 CASE REPORT A rare case of tuberculous mastitis mimicking breast carcinoma Richmond Ronald Gomes* Department of Medicine, Ad-din Women’s Medical College and Hospital, Dhaka, Bangladesh Received on: 13 June 2020; Revised on: 15 July 2020; Accepted on: 01 August 2020 ABSTRACT There have been an increasing number of tuberculosis (TB) cases worldwide, but TB of the breast remains rare. In rare cases, this is seen with a cutaneous manifestation of erythema nodosum. We report the case of a 33-year-old woman with TB of the left breast accompanied by erythema nodosum on the anterior aspect of both lower legs and dorsum of feet. Due to her poor clinical response to conventional therapy, and the histopathological findings of fine-needle aspiration cytology with epithelioid granuloma with caseation, there were strong indications of TB. She received antituberculous therapy (ATT) for 6 months. During her follow-up examination after 6 months, no evidence of either residual or recurrent disease was present. Histopathological features and a high index of clinical suspicion are necessary to confirm a diagnosis of TB of the breast. ATT with or without simple surgical intervention is the core treatment. Keywords: Antituberculous therapy, Caseation, Erythema nodosum, Granuloma, Tuberculosis INTRODUCTION Tuberculosis (TB) is one of the leading infectious diseases worldwide. Extrapulmonary TB involving the breast is extremely rare. It often mimics breast carcinoma and pyogenic breast abscess clinically and radiologically,maybothcoexist.Vulnerabilitytobreast TB is increased in women who are young, married, multiparous and who breastfeed.[1] Histopathological examination using fine-needle aspiration cytology (FNAC) may reveal caseating epithelioid cell granulomas and acid-fast bacilli (AFB).Although the presence of an acid-fast stain or culture is essential to confirm diagnosis, it does not give a positive result in most patients.[2,3] Molecular detection of Mycobacterium tuberculosis by polymerase chain reaction can be particularly useful in the validation of a diagnosis of TB in clinical settings where the diagnosis is uncertain.[3,4] Diagnosis is usually based on high index of suspicion, findings of granulomatous lesion with Langhans’ giant cells, TB culture, and response to antitubercular therapy (ATT). We report a case of TB of the breast associated with a cutaneous manifestation of erythema nodosum. CASE REPORT A 33-year-old married, recently detected diabetic (on metformin), HIV-negative housewife presented at medicine outpatient, Ad-din Women’s Medical College and Hospital, Dhaka, with fever, painful swelling over both shin and dorsum of the feet, bilateral knee, and ankle pain for 8 days. She also gave a history of gradually growing painful discharging lump over her left breast for the past 1 month with on and off undocumented low-grade fever. For the past 8 days, fever became high grade, intermittent (maximum recorded 103°F) associated with chills and rigor and subsided temporarily after taking antipyretic. She did not have any personal medical history of TB or diabetes mellitus. She also neither had family history of breast cancer nor had any contact history with a patient with active TB. She also denied any cough, weight loss, night sweat, anorexia, and Available Online at www.ijms.co.in Innovative Journal of Medical Sciences 2020; 4(3):1-5 ISSN 2581 – 4346 *Corresponding Author: Dr. Richmond Ronald Gomes, E-mail: rrichi.dmc.k56@gmail.com
  • 2. Gomes: Tuberculous mastitis IJMS/Jul-Sep-2020/Vol 4/Issue 3 2 bloody diarrhea. She was immunized as per EPI schedule. With these complaints, she visited a local physician and got 7 days second-generation oral cephalosporin without any improvement. She had a 3-year-old child. On admission, she had a body temperature of 102°F, blood pressure of 126/68 mmHg, a pulse rate of 89/min, and a respiratory rate of 19/min. On physical examination, there was a firm, erythematous, mass of 5 × 6 cm with brownish discharge over the upper outer quadrant of her left breast accompanied by retraction of adjacent skin. Mass was not fixed to underlying structure or overlying skin. Nipple, areola was normal. There was also a firm, non-tender mobile lymph node over left medial axilla. Dark reddish plaque skin lesions were found over both lower legs and the dorsal aspect of her feet. Both ankle and knee joints were also red, swollen. There was also painful restriction of both active and passive movement in these joints. No other joints or axial skeleton was involved. Her blood test results showed the following: Hb% 9.3 gm/dl, MCV – 81, MCH 29,white blood cells at 15.20 × 103 /μL, neutrophils at 77.3%, lymphocytes at 12.7%, platelets at 418 × 103 /μL, C-reactive protein at 86.8 mg/dL (normal range ≤5), and an erythrocyte sedimentation rate during the 1st h of 70 mm/h (normal ≤12). Peripheral blood film revealed normocytic normochromic anemia with neutrophilic leukocytosis. Her blood culture revealed no growth, while her chest radiography was unremarkable. MT was positive with induration 14 mm after 72 h. ALT was 29 U/L, serum calcium was 8.4 mg/dl, and random blood sugar was 13.8 mmol/L. An ultrasonography of our patient’s left breast showed a lump measuring about 5 × 5 cm, which was conglomerated, with an irregular margin with hypoechoic heterogeneous echogenicity, and with a left axillary lymph node. A core needle aspiration biopsy of her left breast was also performed. Under the microscope, this section of her left breast showed chronic mastitis mixed with granulation tissue and numerous foreign body giant cells but with no evidence of malignancy [Figure 1]. Background consisted of necrotic material and fibrinous exudate. A culture of the wound tissues failed to grow any organisms. Stains for AFB were negative. Discharge for GeneXpert Figure 1: Hematoxylin and eosin stain of our patients breast tissue, showing giant cell (arrow) and inflammatory cells Figure 2: Healed ulcer with sinuses after 2 months of ATT therapy Figure 3: After 6 months of completion of ATT therapy
  • 3. Gomes: Tuberculous mastitis IJMS/Jul-Sep-2020/Vol 4/Issue 3 3 TB was not sent due to come unavoidable logistic support. A dermatologist was consulted regarding the dark reddish plaque skin lesions and treated conservatively with NSAIDs. Our final diagnosis tubercular mastitis was relied on clinical suspicion, histopathological tissue findings, and failure to respond to conventional antibiotic therapy. She was put on a 6-month course of antitubercular therapy with a 2-month intensive phase ofrifampicin,isoniazid,ethambutol,andpyrazinamide without steroid followed by a consolidation phase of rifampicin and isoniazid for another 4 months. After undergoing 4 months of antituberculous treatment, her left breast mass and axillary node were gradually reduced [Figure 2]. Although acid-fast stain showed no tubercle bacilli, her ATT was continued. Her left breast mass gradually became smaller and then regressed. She was treated for 6 months without any further complication [Figure 3]. She was regularly followed up for another 6 months and no evidence of the recurrence of her disease was noted. DISCUSSION TB remains one of the leading causes of death from infectious diseases worldwide. Despite the fact that it can affect any organ or site of the body, the breasts, skeletal muscles, and spleen are the most resistant to TB.[5,6] TB comprises approximately 0.025%–0.1% ofallsurgicallytreateddiseasesofthebreast,butthis ratio is higher in underdeveloped countries.[7] The first description of mammary TB was given by Sir Astley Cooper in 1829.[5] He described TB mastitis as “scrofulous swelling” in the bosom of young women.Although breast TB is primarily considered a disease of the developing world, a steady increase in the incidence of the disease has also been seen in developed countries. This is probably because of the migration of the infected population from endemic zones and an increasing number of patients who are immunocompromised.[8] Tuberculous mastitis is more commonly seen in females of reproductive age group, however, especially during the lactation period, when they are more susceptible since the lactating breast is more vascular and predisposed to trauma.[4,5] Both breasts are reported to be involved with equal frequency. Bilateral disease is rare, occurring in 3% of patients.[5] The duration of symptoms varies from a few months to several years, but in most instances, it is less than a year. Constitutional symptoms such as fever, weight loss, night sweats, or a failing of general health are infrequently encountered[2] and are present 20% of cases. Our patient presented only a month history of breast lump without much constitutional symptoms. Its clinical manifestations are variable. Patients usually have a positive tuberculin skin test[9] so as our patient had. ThecommonpresentationofbreastTBisalumpinthe breast with or without ulceration, may associate with the sinus. Other presentations are diffuse nodularity andmultiplesinuses.Multiplelumpsarelesscommon. Pain in the lump is present more frequently in breast TB cases than in breast carcinomas but our patient had painful breast lump. The involvement of the nipple and the areola is rare inTB. Fixation of the skin, which resembles a neoplastic lesion, may also be present but nipple discharge is uncommon.[10] Associated axillary lymphadenopathyisfoundinsomepatients[1,3,11] asour patient had. Other uncommon presentations include; a typical undermined tuberculous ulcer, purulent discharge from the nipple or with a fluctuant swelling which, if inadvertently incised, produces a discharging ulcer.[5,12] Both breasts can be affected equally but bilateralinvolvementisveryuncommon.Althoughthe upper outer quadrant seems to be the most frequently involved site due to its proximity to the axillary nodes, any area of the breast can be affected.[9] Lung lesions (active or healed) on radiographic examination are rare now. Mammography is of limited use since the findings are often indistinguishable from a malignancy[12] and young patients have highly dense breast tissue. Coexisting TB and carcinoma of the breast were reported byAlzaraa et al.[13] TB of the breast is mainly classified according to its primary and secondary forms. Although it was initially believed that as much as 60% of breast TB was primary, it is now accepted that mammary TB is almost invariably secondary to a lesion elsewhere in the body. Primary infection of the breast, however, through abrasions in the skin or through the duct openings on the nipple is a possibility. The most common mode of infection is thought to be retrograde lymphatic spread from the pulmonary focus through the paratracheal and internal mammary lymph nodes. Hematogenous
  • 4. Gomes: Tuberculous mastitis IJMS/Jul-Sep-2020/Vol 4/Issue 3 4 spread and direct extension from contiguous structures are other modes of infection.[5] Breast TB was originally classified by McKeon et al.[14] into the following categories: (a) Acute miliary type – rare, due to blood borne infection in miliary TB; (b) nodular type – the most common type, which presents as a localized lump with or without sinuses in one quadrant of the breast; (c) disseminated type – involving the entire breast with multiple sinuses; (d) sclerosing type – minimal caseation and extensive hyalinization of the stroma, shrinkage of the breast tissue with early skin retraction, and late sinus formation; clinically, this type is indistinguishable from carcinoma; and (e) tuberculous mastitis obliterans – a rare form due to intraductal infection with fibrosis and obliteration of the ductal system; sinus formation is infrequent.[3,5,14] Mantoux testing does not offer definitive diagnosis, but confirms exposure of the patient to tubercle bacilli. Radiological imaging modalities such as mammography and ultrasonography are unreliable in distinguishing breast TB from breast carcinoma. Similarly, computed tomography (CT) scan and MRI do not give a conclusive diagnosis without histopathological confirmation. CT scan is useful in differentiating between the primary and secondary forms.Itisalsohelpfulinevaluatingtherelationship between deeply located lesions with the chest wall and pleura and in detecting parenchymal lesions of the lung. As such it provides valuable guides to surgery and in defining the extent of the disease, including the involvement of the chest wall.[11,15] The demonstration of AFB from the lesions is usually difficult.[16] In tuberculous mastitis, AFB are identified only in 12% of the patients. Our patient also did not show any AFB in the lesion. Therefore, clinical suspicion and demonstration of caseating granulomas with Langhans’ giant cells from the breast tissue and involved lymph nodes may be sufficient for the diagnosis. In TB endemic countries, the finding of granuloma in FNAC warrants empirical treatment for TB even in the absence of positive AFB and without culture results.[16,17] Detailed histological evaluation is, however, mandatory to rule out a coexisting carcinoma. Core needle aspiration biopsy from our patients left breast revealed caseation, epithelioid giant cells without any evidence of malignancy. FNAC is very useful and it is a promising technique in expert hands.[17] Abiopsy is mandatory for confirmation of diagnosis. Antituberculous chemotherapy is still the main treatment for breast TB, and no specific guidelines are available for this kind of treatment. The disease should be treated as any other form of extrapulmonary TB. ATT comprises rifampicin, isoniazid, pyrazinamide, and ethambutol for the initial 2 months, which is then followed by rifampicin and isoniazid for another 4 months. The extension of ATT from 12 to 18 months is required in patients with slow clinical response, and complete resolution is obtained in most patients. Our patient showed response in 6 months so further extension of therapy was not given. FNAC should be repeated to confirm that the residual mass is fibrotic. In refractory cases that lead to breast destruction, a simple mastectomy may be performed.[1,3,9,11] Radical mastectomy is best avoided unless there is a coexisting malignancy.[5,12] The duration of follow-up after therapy is variable. In a study by Shinde et al., all patients were followed up for a minimum of 2 years to determine that they were free of the disease after therapy.[1] After complete ATT, residual lumps localized to a quadrant should be excised through segmental or sector mastectomy. Aspiration or surgical drainage may be required in some cases. The cutaneous involvement of TB is rare. Underlying systemic involvement of TB is often seen in cutaneous TB, especially in children. Cutaneous TB is classified as true TB or tuberculids. True cutaneous TB is composed of tuberculous chancre, miliary TB, lupus vulgaris, scrofuloderma, TB verrucosa cutis, tuberculous metastatic abscess, and orificial TB. Tuberculids are delayed sensitivity reactions to M. tuberculosis in patients with a strong immune response. Tuberculids include lichen scrofulosorum and papulonecrotic tuberculid. Facultative tuberculids consist of erythema induratum and erythema nodosum. Erythema induratum is a recurrent, painful subcutaneous nodule usually on the posterior aspect of the leg. Biopsy shows lobular panniculitis with vasculitis and granulomatous inflammation. Erythema nodosum is a painful subcutaneous nodule, mostly found on the anterior
  • 5. Gomes: Tuberculous mastitis IJMS/Jul-Sep-2020/Vol 4/Issue 3 5 aspect of the leg. Biopsy shows septal panniculitis with an absence of vasculitis and usually without granuloma. Erythema nodosum often occurs in associationwithagranulomatousdisease,including sarcoidosis, TB, and granulomatous colitis. TB remains an important cause of erythema nodosum in endemic countries.[18] CONCLUSION In endemic TB regions, a painful breast mass with cutaneous manifestation of erythema nodosum is clinically relevant to determine a diagnosis of breast TB. To conclude, diagnosis of tuberculous mastitis is usually based on high index of suspicion, finding of granulomatous lesion with Langhans’ giant cells, and response to ATT. FNAC and biopsy may also be inconclusive. AFB is not seen in most cases. Prompt diagnosis and adequate treatment can avoid unnecessary operation in these patients. REFERENCES 1. Shinde SR, Chandawarkar RY, Deshmukh SP. Tuberculosis of the breast masquerading as carcinoma: A study of 100 patients. World J Surg 1995;19:379-81. 2. Akçay MN, Sağlam L, Polat P, Erdoğan F, Albayrak Y, Povoski SP. Mammary tuberculosis--importance of recognition and differentiation from that of a breast malignancy: Report of three cases and review of the literature. World J Surg Oncol 2007;5:67. 3. Tewari M, Shukla HS. Breast tuberculosis: Diagnosis, clinical features and management. Indian J Med Res 2005;122:103-10. 4. Marchetti G, Gori A, Catozzi L, Vago L, Nebuloni M, Rossi MC, et al. Evaluation of PCR in detection of Mycobacterium tuberculosis from formalin-fixed, paraffin-embedded tissues: Comparison of four amplification assays. J Clin Microbiol 1998;36:1512-7. 5. Banerjee SN, Ananthakrishnan N, Mehta RB. Tuberculous mastitis: A continuing problem. World J Surg 1987;11:105-9. 6. Madhusudhan KS, Gamanagatti S. Primary breast tuberculosis masquerading as carcinoma. Singapore Med J 2008;49:e3-5. 7. Kalac N, Ozkan B, Bayiz H, Dursun AB, Demirag F. Breast tuberculosis. Breast 2002;11:346-9. 8. Zandrino F, Monetti F, Gandolfo N. Primary tuberculosis of the breast. A case report. Acta Radiol 2000;41:61-3. 9. Wilson JP, Chapman SW. Tuberculous mastitis. Chest 1990;98:1505-9. 10. Fadaei-Araghi M, Geranpayeh L, Irani S, Matloob R, Kuraki S. Breast tuberculosis: Report of eight cases. Arch Iran Med 2008;11:463-5. 11. Khanna R, Prasanna GV, Gupta P, Kumar M, Khanna S, KhannaAK. Mammary tuberculosis: Report on 52 cases. Postgrad Med J 2002;78:422-4. 12. Al Soub H, Chacko K. Tuberculous mastitis: A rare disease. Br J Clin Pract 1996;50:50-1. 13. Alzaraa A, Dalal N. Coexistence of carcinoma and tuberculosis in one breast.World J Surg Oncol 2008;6:29. 14. Mckeown KC, Wilkinson KW. Tuberculous disease of the breast. Br J Surg 1952;39:420-9. 15. Kervancioğlu S, Kervancioğlu R, Ozkur A, Şirikçi A. Primary tuberculosis of the breast. Diagn Interv Radiol 2005;11:210-2. 16. Kakkar S, Kapila K, Singh MK, Verma K. Tuberculosis of the breast. A cytomorphologic study. Acta Cytol 2000;44:292-6. 17. Mehrotra R. Fine needle aspiration diagnosis of tuberculous mastitis. Indian J Pathol Microbiol 2004;47:377-80. 18. Sethuraman G, Ramesh V, Raman M, Sharma VK. Skin tuberculosis in children: Learning from India. Dermatol Clin 2008;26:285-94.