scholarly journals Intussuscepted Sigmoid Colonic Lipoma Mimicking Carcinoma Rectum

2016 ◽  
pp. 56-58
Author(s):  
Sharmistha Roy ◽  
Samiron Kumar Mondal ◽  
Tapash Kumar Maitra
Keyword(s):  
Sigmoid Colon ◽  
Female Patient ◽  
Rare Condition ◽  
Benign Neoplasm ◽  
Colonic Lipoma ◽  
Carcinoma Rectum

Adult colorectal intussusception is a relatively rare condition. It is different from that of a child in that, most cases have an organic etiology like a malignant or benign neoplasm. This is a 40 year female patient presenting with passage of blood and mucous per rectum later diagnosed as sigmoidorectal intussusception due to submucous lipoma in sigmoid colon that was protruding through anus giving the appearance of a large polypoid rectal growth.Birdem Med J 2015; 5(1) Supplement: 56-58

scholarly journals Choledochal Cyst: A Report of a Rare Disease

1970 ◽  
Vol 13 (1) ◽  
pp. 120-122
Author(s):  
Md Billal Alam ◽  
Shormistha Biswas ◽  
Ratan Das Gupta ◽  
Anup Kumar Shaha ◽  
Shahidur Rahman ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Bile Duct ◽  
Rare Disease ◽  
Female Patient ◽  
Choledochal Cyst ◽  
Rare Condition ◽  
Abdominal Ultrasound ◽  
Recurrent Pain ◽  
Aneurysmal Dilatation ◽  
Upper Abdomen

Choledochal cyst is an aneurysmal dilatation of the bile duct. It is a rare condition. Here we report a case of choledochal cyst in a 15 year-old female patient. She presented to the out patient clinic with the complaints of recurrent pain and lump in the upper abdomen along with fever for 1 year. The diagnosis was made by abdominal ultrasound complemented by computed tomography. DOI: http://dx.doi.org/10.3329/jom.v13i1.10091 JOM 2012; 13(1): 120-122

scholarly journals Laparoscopic resection of a sigmoid colon lipoma in a young female patient: A case report and review of the literature

2017 ◽  
Vol 13 (3) ◽  
pp. 1303-1306 ◽  
Author(s):  
Georgios I. Panagiotakis ◽  
Alexandros G. Andreou ◽  
Ioannis E. Petrakis ◽  
Maria Tzardi ◽  
Maria Daskalogiannaki ◽  
...  
Keyword(s):  
Case Report ◽  
Sigmoid Colon ◽  
Female Patient ◽  
Laparoscopic Resection ◽  
Young Female ◽  
Review Of The Literature

scholarly journals Vulvar Hemangioma: Case Report

2018 ◽  
Vol 40 (06) ◽  
pp. 369-371
Author(s):  
Janine Silva ◽  
Emily Calife ◽  
João Cabral ◽  
Hildemárzio Andrade ◽  
Ana Gonçalves
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Female Patient ◽  
Surgical Approach ◽  
Benign Neoplasm ◽  
Surgical Excision ◽  
Genital Ulcer ◽  
Emotional Disability ◽  
The Past ◽  
History Of

AbstractHemangioma is a benign neoplasm that may affect the vulva, and it can cause functional or emotional disability. This article reports the case of a 52-year-old female patient with a history of a genital ulcer for the past 3 years and who had undergone various treatments with creams and ointments. The patient was biopsied and diagnosed with vulvar hemangioma and was subsequently submitted to surgical excision of the lesion. We emphasize the importance of following the steps of the differential diagnosis and proceeding with a surgical approach only if necessary.

scholarly journals Báo cáo một trường hợp u cơ trơn nguyên phát ở thận và hồi cứu y văn

2020 ◽  
Author(s):  
Thị Hoài Nam Trịnh
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Renal Tumor ◽  
Benign Neoplasm ◽  
Review Literature ◽  
Solid Mass ◽  
Spindle Cells ◽  
Eosinophilic Cytoplasm

A CASE REPORT OF RENAL LEIOMYOMA AND REVIEW LITERATURE Renal leiomyoma is a benign neoplasm that has been reported frequently in uterus but rarely in kidney. The aim of this study is to show a case report of primary renal leiomyoma and review literature. A 59-year-old female patient presented with an indolent right kidney mass. AbdominalCT Scan showed a well-defined hyperattenuating solid mass, no invade. Microscopically, the lesion showed typical features of leiomyoma, including spindle cells with deeply eosinophilic cytoplasm, arranged in intersecting fascicles. Thetumor cells were diffusely positive with vimentin, SMA and desmin. Keywords: leiomyoma, renal tumor, renal leiomyoma.

scholarly journals Localized Hypertrichosis with Traumatic Panniculitis: A Case Report and Literature Review

2019 ◽  
Vol 11 (2) ◽  
pp. 180-186
Author(s):  
Monthanat Ploydaeng ◽  
Salinee Rojhirunsakool ◽  
Poonkiat Suchonwanit
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Blunt Trauma ◽  
Female Patient ◽  
Hair Growth ◽  
Rare Condition ◽  
Inflammatory Cells ◽  
Growth Cycle ◽  
Local Inflammation

Localized hypertrichosis with traumatic panniculitis is considered a rare condition. Previous articles have reported occurrence in females aged between 20 and 35 years. Possible mechanisms of trauma-induced localized hypertrichosis include hyperemia and angiogenesis induced by local inflammation, which can alter the hair growth cycle. The presence of inflammatory cells and lipomembranous changes on histopathology can support the diagnosis. We herein present a 35-year-old female patient with localized hypertrichosis following blunt trauma.

A Rare Case of Intra Mesenteric Dermoid Cyst

2021 ◽  
Vol 8 (05) ◽  
pp. 275-277
Author(s):  
Vikas Katiar ◽  
Kumar Vineet ◽  
Himanshu Singh ◽  
Sanjay Tripathi ◽  
Vikas Patel
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Female Patient ◽  
Rare Case ◽  
Rare Condition ◽  
Epidermal Cells ◽  
Mild Pain ◽  
Glandular Cells

A dermoid cyst is a teratoma of a cystic nature which can occur wherever a teratoma can occur. Intra mesenteric dermoid cyst is rarest of rare case and even its incidence is not known. Here, we report a case of intra mesenteric dermoid cyst in 21 yr. old female patient who presented to us with complain of on & off mild pain in abdomen for last 2 years. Intra mesenteric dermoid cyst is a rare condition and when presented with symptoms, it should be operated upon for improving patient’s overall wellbeing. Dermoids belong to the group of congenital cystic tumours developing from an embryonic rest. Such tumours vary from those which contain only epidermal cells to those containing various dermal derivatives, such as glandular cells (sebaceous), and even hair and teeth. So, they vary from pure epidermoids to dermoids and then through the teratoid tumours to the teratomas. These tumours can arise wherever two ectodermal surfaces fuse together in the developing embryo when an ectodermal implant is retained deep in the surface.”1 Intra mesenteric dermoid is very rare and no previous case report regarding intra mesenteric dermoid was found.

An intussuscepting colonic lipoma causing prolapse of the sigmoid colon in an adult

2019 ◽  
Vol 80 (3) ◽  
pp. ii-ii
Author(s):  
Charles T West ◽  
Adam Pilarski ◽  
Daniel White ◽  
David Ricketts
Keyword(s):  
Sigmoid Colon ◽  
Colonic Lipoma

scholarly journals Concurrent Vitiligo and Psoriasis

2012 ◽  
Vol 10 (1) ◽  
pp. 72-76 ◽  
Author(s):  
D Karn ◽  
S KC
Keyword(s):  
Medical Journal ◽  
Literature Review ◽  
Female Patient ◽  
Rare Condition ◽  
Autoimmune Disorders ◽  
Rare Occurrence ◽  
Single Patient ◽  
Dermatology Department

Coexistence of vitiligo and psoriasis in a single patient is a rare occurrence. The exact pathogenesis of this coexistence is obscure. Various autoimmune disorders are reported to occur more frequently in patients with both diseases. A case of this interesting coexistence seen on a 26 year old female patient who presented to the dermatology department of Dhulikhel hospital is presented here. She also had hypothyroidism. The possible pathogenesis and literature review of this rare condition is discussed here. KATHMANDU UNIVERSITY MEDICAL JOURNAL  VOL.10 | NO. 1 | ISSUE 37 | JAN - MAR 2012 | 83-84 DOI: http://dx.doi.org/10.3126/kumj.v10i1.6921

scholarly journals Juxtaglomerular Cell Tumor: Reviewing a Cryptic Cause of Surgically Correctable Hypertension

2019 ◽  
Vol 13 (1) ◽  
pp. 7-12 ◽  
Author(s):  
Rafid Inam ◽  
Jason Gandhi ◽  
Gunjan Joshi ◽  
Noel L. Smith ◽  
Sardar Ali Khan
Keyword(s):  
Early Recognition ◽  
Rare Condition ◽  
Benign Neoplasm ◽  
Juxtaglomerular Apparatus ◽  
Cell Tumor ◽  
Surgical Removal ◽  
Juxtaglomerular Cell ◽  
Juxtaglomerular Cell Tumor ◽  
High Index Of Suspicion ◽  
The Impact

Juxtaglomerular cell tumor (JGCT), or reninoma, is a typically benign neoplasm generally affecting adolescents and young adults due to modified smooth muscle cells from the afferent arteriole of the juxtaglomerular apparatus. Patients experience symptoms related to hypertension and hypoka-lemia due to renin-secretion by the tumor. MRI, PET, CT, and renal vein catheterizations can be used to capture JGCTs, with laparoscopic ultrasonography being most cost-efec-tive. Surgical removal is the best option for management; electrolyte imbalances are a potential complication which may be assuaged via pre-surgical administration of aliskiren, a renin inhibitor. Considering the vast etiology for hypertension and rarity of JGCT, the diagnosing physician must have a high index of suspicion for JGCT. Early recognition and management can help prevent cardiovascular or pregnancy complications and fatalities, vascular invasion and metastasis, improve quality of life, and limit socioeconomic liabilities. Herein we review the epidemiology, genetics, histopathol-ogy, clinical presentation, and management of this rare condition. The impact of genetics on prognosis warrant further research.

scholarly journals Adrenal schwannoma in a female patient; A rare benign neoplasm: Case report and literature review

2020 ◽  
Vol 74 ◽  
pp. 173-176
Author(s):  
Marcos Jafif Cojab ◽  
Jesus Flores Armenta ◽  
Diego L. Jorge ◽  
Rodrigo Sanchez Hernandez ◽  
Oscar Cervantes Gutierrez ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Female Patient ◽  
Benign Neoplasm
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