scholarly journals Fibrous Pseudotumor of Para Testicular Region; A Rare Clinical Entity

2021 ◽  
Vol 2 (2) ◽  
pp. 62-64
Author(s):  
Kamran Hassan Bhatti
Keyword(s):  
Tunica Albuginea ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Tunica Vaginalis ◽  
Testicular Tumors ◽  
Palpable Mass ◽  
Case Presentation ◽  
Scrotal Swelling ◽  
Asian Male ◽  
Rare Benign Tumour

Background Para testicular pseudotumor is a rare benign tumour originating most commonly from tunica vaginalis, less commonly from tunica albuginea, epididymis, and the spermatic cord. Case Presentation We present a case of a 27- year old Asian male patient who presented with painless palpable mass in the left hemiscrotum. Scrotal ultrasonography showed well-defined lobulated solid left Para testicular lesion closely related to the tunica/epididymis with specks of calcification within the lesion. Scrotal exploration and excision of the tumour was performed. Histopathology Findings revealed fibrous pseudotumor. Conclusion Para testicular fibrous pseudotumor is a rare clinical entity in young adults, scrotal swelling mimics testicular tumour. Preoperative diagnosis is a pitfall. Histopathology is the only way to establish diagnosis. Keywords: Para testicular; Tumors; Surgical exploration; Orchiectomy.

scholarly journals Complicated Amyand’s Hernia in a Neonate

2014 ◽  
Vol 3 (3) ◽  
Author(s):  
Parkash Mandhan ◽  
Talal Al Rayes ◽  
Mansour J Ali ◽  
Mahmoud Aldhaheri
Keyword(s):  
Inguinal Hernia ◽  
Vermiform Appendix ◽  
Clinical Entity ◽  
Amyand’S Hernia ◽  
Rare Clinical Entity ◽  
Hernia Sac ◽  
Surgical Exploration ◽  
Dysmorphic Features ◽  
Scrotal Swelling

Amyand’s hernia is a rare clinical entity in which the vermiform appendix is present within the inguinal hernia sac. Here, we report a 5-day-old neonate with dysmorphic features referred to us with a tender irreducible right inguino-scrotal swelling. Surgical exploration showed gangrenous appendix with a peri-appendicular abscess in the inguinal hernia sac. Appendectomy and right herniotomy was performed.

A rare testicular tumor: primary carcinoid tumor

2019 ◽  
Vol 105 (6) ◽  
pp. NP20-NP23
Author(s):  
Tchin Darré ◽  
Brahima Doukouré ◽  
Mohamed Kouyaté ◽  
Toukilnan Djiwa ◽  
Doh Kwamé ◽  
...  
Keyword(s):  
Carcinoid Tumor ◽  
Testicular Tumor ◽  
Undifferentiated Carcinoma ◽  
Placental Alkaline Phosphatase ◽  
Review Of The Literature ◽  
Testicular Tumors ◽  
Case Presentation ◽  
Primary Carcinoid Tumor ◽  
Scrotal Swelling ◽  
Neuroendocrine Carcinomas

Background:Primary carcinoid tumors are rare and constitute 0.23% of all testicular tumors. We report a case of primary carcinoid tumor of testicular localization, with a review of the literature.Case presentation:A 29-year-old man, without specific ascendants, consulted the urology department for progressive scrotal swelling of 6 months, associated with pain. After surgery, histology showed diffuse tumor proliferation composed of small round monotone cells with hyperchromatic nuclei evoking undifferentiated carcinoma. Immunohistochemistry showed that tumor cells were positive for chromogranin A and negative for placental alkaline phosphatase and α-fetoprotein.Conclusion:Primary neuroendocrine carcinoma of the testis is a very rare malignant tumor. Immunohistochemistry contributes to its diagnosis in relation to other metastatic neuroendocrine carcinomas, carcinoid tumor teratomas, seminoma, and Sertoli cells.

scholarly journals Bronchoesophageal fistula secondary to esophageal diverticulum in an adult: a case report and literature review

2021 ◽  
Vol 49 (2) ◽  
pp. 030006052199223
Author(s):  
Xiaolin Zhang ◽  
Hongmei Jiao ◽  
Xinmin Liu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Respiratory Infections ◽  
Relevant Literature ◽  
Rare Condition ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Esophageal Diverticulum ◽  
Bronchoesophageal Fistula ◽  
Fatal Complications

Esophageal diverticulum with secondary bronchoesophageal fistula is a rare clinical entity that manifests as respiratory infections, coughing during eating or drinking, hemoptysis, and sometimes fatal complications. In the present study, we describe a case of bronchoesophageal fistula emanating from esophageal diverticulum in a 45-year-old man who presented with bronchiectasis. We summarize the characteristics of this rare condition based on a review of the relevant literature.

scholarly journals Primary tubercular caecal perforation: a rare clinical entity

BMC Surgery ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Devendra K Jain ◽  
Gaurav Aggarwal ◽  
Parvinder S Lubana ◽  
Sonia Moses ◽  
Nitin Joshi
Keyword(s):  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Caecal Perforation

scholarly journals Cartilaginous Choristoma of the Gingiva: A Rare Clinical Entity

2014 ◽  
Vol 2014 ◽  
pp. 1-4
Author(s):  
Ramalingam Suganya ◽  
Narasimhan Malathi ◽  
Subramani Vijaya Nirmala ◽  
Chinnaswami Ravindran ◽  
Harikrishnan Thamizhchelvan
Keyword(s):  
Connective Tissue ◽  
Histopathological Examination ◽  
Clinical Entity ◽  
Fibrous Connective Tissue ◽  
Rare Clinical Entity ◽  
Normal Cells ◽  
Connective Tissue Stroma

Choristomas are rare entities which are aggregates of microscopically normal cells or tissues in aberrant locations. They are a “heterotopic” rest of cells, as they appear as a tumor-like mass. Herein we report a case of cartilaginous choristoma in a 54-year-old male who presented with a swelling on right lower gingiva. The histopathological examination revealed features of a well circumscribed mass of mature cartilage in a dense fibrous connective tissue stroma.

scholarly journals Role of Immunotherapy in Pulmonary Angiosarcoma: A Case Report

2021 ◽  
pp. 797-801
Author(s):  
Quang Tien Nguyen ◽  
Anh Tuan Pham ◽  
Thuy Thi Nguyen ◽  
Tam Thi Thanh Nguyen ◽  
Ky Van Le
Keyword(s):  
Case Report ◽  
Poor Prognosis ◽  
Checkpoint Inhibitor ◽  
Therapeutic Strategies ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Excellent Response ◽  
First Case

Pulmonary angiosarcoma is a rare clinical entity with a poor prognosis and no established therapeutic strategies. We present the first case to our knowledge of metastatic pulmonary angiosarcoma, treated with checkpoint inhibitor immunotherapy, and have an excellent response. Until now, patient has been treated with immunotherapy for 1 year, and his disease is stable and well-tolerated.

Acquired postganglionic cholinergic dysautonomia – A rare clinical entity

2021 ◽  
Vol 1 (2) ◽  
pp. 352
Author(s):  
MeenaChembil Kakkitampara ◽  
Madhukar Mohan ◽  
AnjuSivadasa Raju
Keyword(s):  
Clinical Entity ◽  
Rare Clinical Entity

scholarly journals Comprehensive analysis of ectopic mandibular third molar: a rare clinical entity revisited

2017 ◽  
Vol 13 (1) ◽  
Author(s):  
Yaping Wu ◽  
Yue Song ◽  
Rong Huang ◽  
Jiaan Hu ◽  
Xiaotong He ◽  
...  
Keyword(s):  
Third Molar ◽  
Comprehensive Analysis ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Mandibular Third Molar
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