Browsing by Author "Yadav, ML"

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    A Rare Case of an Adult with Untreated Bladder Exstrophy Presenting with Adenocarcinoma of Urinary Bladder.
    (Educational Society for Excellence, 2017) Gupta, P; Saxena, S; Joshi, N; Nag, BP; Yadav, ML; Mathur, A.
    Untreated bladder exstrophy in an adult is rare, as the defect is obvious and primary reconstruction is usually done in infancy. There are less than 90 reported cases of primary adenocarcinoma in an untreated bladder exstrophy in literature and only two such case reports from India. We report the case of adenocarcinoma in a 29 year old male with untreated bladder exstrophy to highlight the extreme rarity, yet distinct possibility and challenges faced in surgical management of such cases.
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    A rare case report of primary tuberculosis of tongue
    (Educational Society for Excellence, 2016) Sharma, MK; Joshi, N; Yadav, ML; Agarwal, T
    Tuberculosis is an infectious disease that has displayed increasing incidence in the last decades. In the ENT area, the most common onset is cervical lymphadenitis, which accounts for 95% of ENT cases. The posterior pharyngeal wall, tonsillar pillars, sidewalls, soft palate, and tongue are the least probable locations. A 40 year old male presented in the ENT OPD with a growth at base of tongue, involving the lateral sulcus, anterior tonsillar pillar and lower pole of tonsil left side. A biopsy was taken from the same area and sent for histopathological examination with a strong clinical suspicion of squamous cell carcinoma. The final histopathological diagnosis was tuberculosis of tongue. The patient showed good response on ATT.
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    Sarcomatoid Renal Cell Carcinoma: A Rare Case Report
    (Educational Society for Excellence, 2017) Gupta, P; Saxena, S; Joshi, N; Nag, BP; Yadav, ML; Mathur, A.
    Sarcomatoid renal cell carcinoma (SRCC) is an aggressive variant of renal cell carcinoma. It is thought to originate predominantly from clear cell carcinoma through de-differentiation. It is a rare entity constituting about 1-5% of all renal malignant neoplasms and is more commonly associated with conventional (clear cell) renal cell carcinomas. We report a case of 62 years old male who presented with complaints of haematuria and abdominal pain. The histopathology confirmed sarcomatoid renal cell carcinoma.
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    Sertoli cell nodule of the testis: An incidental finding
    (Educational Society for Excellence, 2017) Manisha, Bhardwaj; Narayani, Joshi; Nag, BP; Yadav, ML
    The case of a 21year old man with complaints of pain in the lower abdomen reported in the surgery OPD. USG showed a case of undescended testis. A radical Orchidectomy was performed and the specimen was received in the department of pathology. Grossly the testis was normal .Microscopic examination showed the encapsulated nodule composed of tubules lined by immature Sertoli cells interspersed with tubules and Spermatogonia and an interwoven network of hyalinised basement membrane having foci of calcification. The findings were identical to those of a Sertoli cell nodule-A typically microscopic encapsulated lesion commonly detected in crypt orchid testes. Here we present a case of undescended testis where incidentally we found all the features of sertoli cell nodule
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    Unusual presentation of a case of intra cystic papillary carcinoma of breast
    (Educational Society for Excellence, 2017) Gupta, P; Joshi, N; Nag, BP; Yadav, ML; Mathur, A
    The term “intra cystic papillary ductal carcinoma in situ”, has recently changed and is now more appropriately referred to as “intra cystic papillary carcinoma’’ constituting only 0.5% to 1% of all breast cancers. Herein, we discuss an unusual case of intra cystic in situ papillary carcinoma of breast in a postmenopausal woman, the diagnosis of which was made on histopathology. So careful histopathological evaluation is the mainstay to arrive at the correct diagnosis to avoid untoward complications related to under diagnosis and/ over diagnosis.
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    Uterus Didelphys presenting with ruptured uterus in third pregnancy: A rare case report
    (Educational Society for Excellence, 2016) Saxena, S; Gupta, P; Akansha; Yadav, ML; Nag, BP; Mathur, A.
    Uterus Didelphys “double uterus” is a congenital malformation that results from complete failure of fusion of the ipislateral paramesonephric ducts during embryonic development. Ideally, diagnosis should be made before pregnancy and labor to prevent adverse outcomes. Here we report a case of uterus didelphys in 30 year old female Gravida4 Para3 Living2 at 31st week of pregnancy admitted with prolonged rupture of membrane, hypovolemic shock and intrauterine fetal death. Postoperative recovery of the mother was uneventful. Clinicians should have high index of suspicion of uterine anomaly when assessing cases of dysfunctional labor to avoid delayed diagnosis and the associated adverse outcome