scholarly journals Actinomycosis of male breast: a rare case report

2020 ◽  
Vol 7 (3) ◽  
pp. 922
Author(s):  
Abhishek Mahadik ◽  
Rontgen Rajakumar ◽  
Nida Khan ◽  
Pragati Singhal
Keyword(s):  
Case Report ◽  
Rare Disease ◽  
Genital Tract ◽  
Wide Local Excision ◽  
Rare Case ◽  
Granulomatous Inflammation ◽  
Breast Lump ◽  
Inflammatory Carcinoma ◽  
Rare Case Report ◽  
Palpable Breast

Actinomyces is a commensal of gastrointestinal and genital tract that may cause subacute or chronic granulomatous inflammation. Primary actinomycosis of breast is an extremely rare disease. It may present as a mass or as discharging fistulae. It is often diagnosed after biopsy. It may mimic inflammatory carcinoma or mastitis. Treatment is with a prolonged course of antibiotic. Authors present a case of a 70-year-old male with a palpable breast lump, that was suspected to be malignant. Wide local excision was performed, histopathology confirmed the diagnosis of actinomycoses breast. Patient was given antibiotics post operatively.

Ectopic Ganglion Cyst Presenting as a Breast Lump: A Rare Case Report

2006 ◽  
Vol 12 (2) ◽  
pp. 170-172
Author(s):  
Mohammad Nadeem ◽  
Arshad H. Malik ◽  
Amit Goyal ◽  
Muhammad H. Niayesh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ganglion Cyst ◽  
Breast Lump ◽  
Rare Case Report

scholarly journals Congenital absence of a part of the fallopian tube: a case report

2016 ◽  
Vol 6 (1) ◽  
pp. 320
Author(s):  
Mukta Agarwal ◽  
Hemali H. Sinha ◽  
. Anamika
Keyword(s):  
Case Report ◽  
Fallopian Tube ◽  
Genital Tract ◽  
Rare Case ◽  
Case Reports ◽  
Female Genital Tract ◽  
Fallopian Tubes ◽  
Rare Occurrence ◽  
Rare Case Report ◽  
Female Genital

Congenital malformations of female genital tract are frequently seen in Gynaecological clinics, incidence being upto 5-6% in cases of infertility. Most of these anomalies are related to uterus and vagina, abnormalities related to ovaries and fallopian tubes are of rare occurrence and the exact incidence of these anomalies are not known, only a few incidental case reports are available in literature. Here, we present a rare case report of absent mid- tubal segment of fallopian tube in a patient of infertility.

scholarly journals Female Hypospadias and Congenital Uterine Müllerian Anomaly with Proved Fertility: A Rare Case Report

2011 ◽  
Vol 3 (3) ◽  
pp. 155-156
Author(s):  
Rekha Choudhary ◽  
Suniti Verma ◽  
Gautam Ram Choudhary
Keyword(s):  
Case Report ◽  
Genital Tract ◽  
Rare Case ◽  
Female Genital Tract ◽  
Urogenital Sinus ◽  
Developmental Relationship ◽  
Rare Case Report ◽  
Mullerian Anomaly ◽  
Primigravid Woman ◽  
Female Genital

ABSTRACT Congenital anomalies of the female genital tract result from müllerian duct anomalies and/or abnormalities of the urogenital sinus or cloaca. Due to the close developmental relationship between the genital and the urinary tracts, association of anomalies in both systems are common. This article reviews the appearance of developmental anomalies of the female urinary (hypospadias) and genital tracts and points out complication associated with bicornuate uterus. A 40-year-old primigravid woman conceived a pregnancy after 10 years of primary infertility. The prenatal course was uncomplicated. At 38 weeks’ gestation, she was successfully delivered by elective low transverse cesarean section.

scholarly journals Primary Small Cell Neuroendocrine Carcinoma of Vagina: A Rare Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Jignasa N. Bhalodia ◽  
Dhiren V. Kapapura ◽  
Malay N. Parekh
Keyword(s):  
Case Report ◽  
Rare Disease ◽  
Tumor Cells ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Neuron Specific Enolase ◽  
Small Cell ◽  
Small Cell Neuroendocrine Carcinoma ◽  
Rare Case Report

Primary small cell neuroendocrine carcinoma of vagina is an extremely rare disease. There have been only 26 previously reported cases in literature. Here, we report a case of primary small cell neuroendocrine carcinoma of vagina. Immunohistochemistry (IHC) showed tumor cells positive for synaptophysin, chromogranin, and neuron-specific enolase (NSE).

scholarly journals Isolated primary echinococcosis of breast: A rare case report

2017 ◽  
Vol 23 (1) ◽  
pp. 15-16
Author(s):  
R. Liubota ◽  
M. Anikusko ◽  
O. Zotov ◽  
R. Vereshchako ◽  
I. Liubota
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Surgical Excision ◽  
Left Breast ◽  
Hydatid Cysts ◽  
Breast Lump ◽  
Rare Case Report ◽  
Endemic Areas ◽  
Specific Symptoms

Isolated echinococcosis or hydatid cyst of breast is very rare disease especially in non-endemic areas. Even in endemic areas, hydatid cysts detects only for 0.27% of all cases of hydatidosis. Diagnosis of hydatid disease is difficult and it is diagnosed after surgical excision in majority cases. We report a case of 39 year old female with isolated hydatid cyst of the left breast that appeared as a painless breast lump without any specific symptoms.

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