scholarly journals The Squamous Vaginal Papillomatosis in Prepubertal Female Twins: A Case Report

2021 ◽  
Vol 28 (2) ◽  
pp. 18
Author(s):  
Evelina Boreikaitė ◽  
Vytautas Bilius ◽  
Elžbieta Bumbul-Mazurek ◽  
Žana Bumbulienė
Keyword(s):  
Case Report ◽  
Informed Consent ◽  
Squamous Epithelium ◽  
Histopathologic Examination ◽  
Fibroepithelial Polyp ◽  
Urethral Meatus ◽  
Pediatric Surgeon ◽  
Twin Sister ◽  
First Case ◽  
Pediatric Urologist

This is the first case describing vaginal papillomatosis with a fibroepithelial polyp of the vulva in a prepubertal girl and vaginal papillomatosis in her twin sister. Parents contacted pediatric urologist regarding their eight-year-old daughter (twin A), who had a growth next to the external urethral meatus. The girl was referred to a pediatric surgeon. The exophytic 3 cm long structure with necrosis on top was found. After obtaining informed consent from girl parents, pediatric surgeon removed the exophytic structure and perform cystoscopy and vaginoscopy for possible changes in the bladder and vagina. Cystoscopy findings were normal. On vaginoscopy, numerous macroscopic papillomatous structures were identified on the cervix and vaginal walls. Vaginal biopsies were performed on the areas affected by papillomatosis. Histopathologic examination showed a fibroepithelial polyp with a central fibrovascular core covered by squamous epithelium and vaginal squamous papillomatosis. The decision was made to perform vaginoscopy on her twin sister (twin B), too. On vaginoscopy, solitary small vaginal papillomas were also found. In this case manifestation of vaginal papillomatosis in twins might have been influenced by inheritance and the same bacterial and viral environment.

scholarly journals Endometritis and Cystic Endometrial Hyperplasia in a Goat

2005 ◽  
Vol 17 (4) ◽  
pp. 393-395 ◽  
Author(s):  
Zaher A. Radi
Keyword(s):  
Case Report ◽  
Caesarean Section ◽  
Endometrial Hyperplasia ◽  
Plasma Cells ◽  
Histopathologic Examination ◽  
Boer Goat ◽  
First Case ◽  
Cellular Debris ◽  
Superficial Epithelium ◽  
Cystic Masses

Histologic examination was performed on uterine biopsy samples of irregular cystic masses noted during caesarean section of a 2-year-old female Boer goat. Histopathologic examination revealed multifocal erosions of the superficial epithelium and multifocal infiltration of the endometrium by widely scattered viable and degenerate neutrophils, lymphocytes, and plasma cells admixed with mild amounts of cellular debris and hemorrhage. The endometrium was markedly expanded by many irregular cystic and hyperplastic glands. This is the first case report of endometritis and cystic endometrial hyperplasia in a goat in North America.

Fibroepithelial polyp of the tonsil: case report of a rare, benign tonsillar lesion

2009 ◽  
Vol 124 (1) ◽  
pp. 111-112 ◽  
Author(s):  
A Farboud ◽  
A Trinidade ◽  
M Harris ◽  
A Pfleiderer
Keyword(s):  
Case Report ◽  
English Language ◽  
Fibroepithelial Polyp ◽  
Disturbed Sleep ◽  
English Language Literature ◽  
First Case ◽  
Language Literature ◽  
Left Tonsil

AbstractObjective:We report the case of a man presenting with a tonsillar mass causing difficult breathing, snoring and disturbed sleep.Method:Case report.Results:The patient was found to have a fibroepithelial polyp of the left tonsil.Conclusion:To our knowledge, this is the first case of its type to be presented in the English-language literature. The case is presented and the tumour and its management are discussed.

scholarly journals Giant Ureteral Fibroepithelial Polyp with Intermittent Prolapse Reaching the Urethral Meatus: A Case Report

2017 ◽  
Vol 13 ◽  
pp. 6-9
Author(s):  
Mohamad El-Haress ◽  
Wael Ghandour ◽  
Marwan Bahmad ◽  
Najla Fakhruddin ◽  
Hussein Fawaz ◽  
...  
Keyword(s):  
Case Report ◽  
Fibroepithelial Polyp ◽  
Urethral Meatus

scholarly journals Prenatal diagnosis of feta noncompaction cardiomyopathy with de novo CALM2 mutation

2021 ◽  
Author(s):  
wen zhang ◽  
xiaohui dai ◽  
Hanmin Liu ◽  
Lei Li ◽  
Shu Zhou ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Exome Sequencing ◽  
Genomic Dna ◽  
De Novo ◽  
Heterozygous Mutation ◽  
Histopathologic Examination ◽  
Noncompaction Cardiomyopathy ◽  
First Case ◽  
Whole Exome

We report what apprears to be the first case of fetal noncompaction cardiomyopathy in both ventricles accompanied by a mutation in the calmodulin gene (CALM2): A 25-year-old woman was referred to our hospital at 25+1 weeks of gestation for evaluation of fetal defects. A postnatal echocardiography showed biventricular noncompaction cardiomyopathy. After terminated the pregnancy, fetal noncompaction cardiomyopathy was comfirmed by autopsy and histopathologic examination. And the whole-exome sequencing of genomic DNA demonstrated a de novo heterozygous mutation (c.389A>G;p.D130G) in CALM2, whereas the parents were normal. In this case report, we highlight the gene mutation in noncompaction cardiomyopathy.

Extension of Nasopharyngeal Lymphoma to the Middle and External Ear

2003 ◽  
Vol 112 (7) ◽  
pp. 644-646 ◽  
Author(s):  
Arie Gordin ◽  
Yehudith Ben-Arieh ◽  
Aviram Netzer ◽  
David Goldenberg ◽  
Avishay Golz
Keyword(s):  
Magnetic Resonance Imaging ◽  
Case Report ◽  
External Ear ◽  
Histopathologic Examination ◽  
Resonance Imaging ◽  
Ear Canal ◽  
Direct Extension ◽  
First Case ◽  
Otoscopic Examination ◽  
Left Middle

We describe a patient with nasopharyngeal lymphoma who was admitted for chemotherapy. At admission, otoscopic examination revealed a large polyp occluding the left external ear canal. The polyp was removed, and histopathologic examination showed the same tumor that was found previously in the nasopharynx. Magnetic resonance imaging showed an infiltrative process that involved the left side of the nasopharynx and extended toward the left middle and external ear. To our knowledge, this is the first case report of a direct extension of nasopharyngeal lymphoma into the middle and external ear.

The first case report of Pembrolizumab inducing thyroiditis and hypophysitis

2020 ◽  
Author(s):  
Rahman Maraqa Sima Abdel ◽  
Robert McMahon ◽  
Anusha Pinjala ◽  
Gastelum Alheli Arce ◽  
Mohsen Zena
Keyword(s):  
Case Report ◽  
First Case

Harel-Yoon syndrome: the first case report from Saudi Arabia

2020 ◽  
pp. 22-27 ◽  
Author(s):  
Alaa AlAyed ◽  
Manar Samman ◽  
Abdul Peer-Zada ◽  
Mohammed Almannai
Keyword(s):  
Saudi Arabia ◽  
Case Report ◽  
First Case

Case Report: Management of a Patient with mTBI and Vestibular Hypofunction with the Binasal Occlusion Technique

2018 ◽  
pp. 87-90
Keyword(s):  
Case Report ◽  
Visual Motion ◽  
Hand Movement ◽  
Motion Sensitivity ◽  
Vestibular Hypofunction ◽  
First Case ◽  
Neurological Exam ◽  
History Of ◽  
Occlusion Technique ◽  
Visual Vertigo

Background: Binasal Occlusion (BNO) is a clinical technique used by many neurorehabilitative optometrists in patients with mild traumatic brain injury (mTBI) and increased visual motion sensitivity (VMS) or visual vertigo. BNO is a technique in which partial occluders are added to the spectacle lenses to suppress the abnormal peripheral visual motion information. This technique helps in reducing VMS symptoms (i.e., nausea, dizziness, balance difficulty, visual confusion). Case Report: A 44-year-old AA female presented for a routine eye exam with a history of mTBI approximately 33 years ago. She was suffering from severe dizziness for the last two years that was adversely impacting her ADLs. The dizziness occurred in all body positions and all environments throughout the day. She was diagnosed with vestibular hypofunction and had undergone vestibular therapy but reported little improvement. Neurological exam revealed dizziness with both OKN drum and hand movement, especially in the left visual field. BNO technique resulted in immediate relief of her dizziness symptoms. Conclusion: To our knowledge, this is the first case that illustrates how the BNO technique in isolation can be beneficial for patients with mTBI and vestibular hypofunction. It demonstrates the success that BNO has in filtering abnormal peripheral visual motion in these patients.

Sign in / Sign up

Export Citation Format

Share Document