Multidisciplinary Approach of a Very Rare Infected Verrucous Carcinoma of the Scrotum

2019 ◽  
Vol 70 (4) ◽  
pp. 1476-1478
Author(s):  
Laura Raducu ◽  
Adelaida Avino ◽  
Cristina-Nicoleta Cozma ◽  
Sorin Nedelea ◽  
Andra-Elena Balcangiu-Stroescu ◽  
...  
Keyword(s):  
Adjuvant Therapy ◽  
Rare Disease ◽  
Chronic Inflammation ◽  
Male Patient ◽  
Multidisciplinary Approach ◽  
Verrucous Carcinoma ◽  
Surgical Excision ◽  
Diagnosis And Treatment ◽  
Wide Surgical Excision ◽  
The Right

Verrucous carcinoma of the scrotum is an extremely rare disease and most cases are thought to result from poor hygiene and chronic inflammation. Currently, it has not been well characterized, the etiology, diagnosis and treatment remaining poorly understood. We present the case of a 50-year-old male patient diagnosed with verrucous carcinoma of the right hemiscrotum. Wide surgical excision was performed. Favorable outcomes can be achieved by surgery, even without any adjuvant therapy, but patients should be carefully followed up.

Verrucous Carcinoma of the Nail Bed

1998 ◽  
Vol 19 (5) ◽  
pp. 327-328 ◽  
Author(s):  
Jean P. Van Geertruyden ◽  
Catherine Olemans ◽  
Marianne Laporte ◽  
Jean-Christophe Noël
Keyword(s):  
Squamous Cell Carcinoma ◽  
Cell Carcinoma ◽  
Squamous Cell ◽  
Verrucous Carcinoma ◽  
Surgical Excision ◽  
Nail Bed ◽  
Wide Surgical Excision ◽  
Epithelioma Cuniculatum

Verrucous carcinoma is a rare, highly keratinizing variant of squamous cell carcinoma of the skin or mucosae characterized by a local aggressiveness but a low potential for metastasis. The plantar form is also known as epithelioma cuniculatum. Fingers and toes are rarely affected, and tumors of the nail bed are exceptional. Clinically, the lesion presents like a wart and is then often misdiagnosed. Treatment of choice is wide surgical excision. A case of verrucous carcinoma of the nail apparatus is presented, and diagnosis is discussed.

scholarly journals A Case of Verrucous Carcinoma of Larynx

2020 ◽  
Vol 23 (2) ◽  
pp. 208-211
Author(s):  
Mahmudul Hassan ◽  
Md Zahedul Alam ◽  
Mohammad Hanif ◽  
Md Rafiqul Islam ◽  
Saif Rahman Khan ◽  
...  
Keyword(s):  
Vocal Cord ◽  
Male Patient ◽  
Anterior Commissure ◽  
Verrucous Carcinoma ◽  
Fiberoptic Laryngoscope ◽  
Laser Excision ◽  
The Right ◽  
Carcinoma Of Larynx

A 50 years old male patient was admitted with complaints of change in voice for 2 years, dry cough 2 month and difficulty in breathing for 1 month. On examination with fiberoptic laryngoscope, an exophytic lesion covered with whitish plaque involving right vocal cord extending from anterior commissure to right arytenoid region, extending upto the right vestibular area and hanging in the subglottic area was seen. Patient was treated with Microlaryngeal Laser excision and the Histopathology report was suggestive of Verrucous Carcinoma of Larynx. Bangladesh J Otorhinolaryngol; October 2017; 23(2): 208-211

scholarly journals Abscess of the right iliopsoas muscle: rare disease and difficulties in its diagnosis

2020 ◽  
Vol 179 (2) ◽  
pp. 63-67
Author(s):  
S. V. Stolov ◽  
M. Yu. Kabanov ◽  
K. V. Semencov ◽  
T. Yu. Yamshchikova ◽  
O. V. Makarova ◽  
...  
Keyword(s):  
Rare Disease ◽  
Inflammatory Disease ◽  
Clinical Case ◽  
Multidisciplinary Approach ◽  
Iliopsoas Muscle ◽  
The Right

The article presents the clinical case of an abscess of the iliopsoas muscle (iliopsoitis), a rare abdominal infectious and inflammatory disease that required a multidisciplinary approach in the diagnosis of this pathology in a multidisciplinary hospital.

scholarly journals Juvenile variant ossifying fibroma of sinonasal region

2020 ◽  
Vol 17 (2) ◽  
pp. 77-81
Author(s):  
Susan Pradhan ◽  
Suman Phuyal ◽  
Dipendra Kumar Shrestha ◽  
Sushil Krishna Shilpakar
Keyword(s):  
Multidisciplinary Approach ◽  
Surgical Excision ◽  
Ossifying Fibroma ◽  
Brown Tumor ◽  
Resonance Imaging ◽  
Transnasal Approach ◽  
Endoscopic Transnasal Approach ◽  
Cranial Fossa ◽  
The Right ◽  
Stony Hard

Juvenile variant ossifying fibroma of sinonasal region is an extremely rare benign fibro-osseous lesion which is locally aggressive. A 21-year-old male presented with significant proptosis of right eye with stony-hard lump in the middle upper aspect of the right orbit and base of the nose. CT scan of head revealed a non-enhancing expansile lesion in right ethmoidal cells consistent with chronic ethmoidal mucocele. However Magnetic Resonance Imaging of brain revealed enhancing lesion in right ethmoid and frontal sinus extending up to anterior cranial fossa. He underwent right frontal craniotomy with surgical excision of tumor wherein cystic brown tumor of frontal and ethmoidal sinus was found. The procedure was supplemented with endoscopic transnasal approach. Histopathology report suggested an ossifying fibroma. This case highlights the importance of clinical, imaging and histopathological features of ossifying fibroma occurring in the sinonasal tract for better diagnosis and treatment through a multidisciplinary approach.

scholarly journals A case series on management of scar endometriosis following C-sections

2019 ◽  
Vol 6 (7) ◽  
pp. 2621
Author(s):  
Tharun Ganapathy Chitrambalam ◽  
Sidhu Sekhar ◽  
Jeyakumar S. ◽  
Koshy Mathew Panicker
Keyword(s):  
Cesarean Section ◽  
Medical Treatment ◽  
Case Series ◽  
Uterine Cavity ◽  
Surgical Excision ◽  
Diagnosis And Treatment ◽  
Surgical Scar ◽  
Scar Endometriosis ◽  
Wide Surgical Excision ◽  
Surgical Conditions

Endometriosis is presence of functioning endometrial tissue outside the uterine cavity. Endometriosis can sometimes occur in a previous surgical scar. Scar endometriosis is rare and difficult to diagnose. It mostly follows obstetrical and gynecological surgeries. This condition is often confused with other surgical conditions. We are reporting 5 cases of scar endometriosis following cesarean section, some of which were misdiagnosed as stitch granuloma initially. Medical treatment was not helpful. All 5 patients required wide surgical excision of the lesion. The pathogenesis, diagnosis and treatment of this condition are being discussed.

Verrucous Carcinoma due to Arsenic Ingestion in a Psoriasis Patient

2012 ◽  
Vol 16 (6) ◽  
pp. 445-447 ◽  
Author(s):  
Jian-Wei Zhu ◽  
Min Zheng
Keyword(s):  
Pulmonary Embolism ◽  
Male Patient ◽  
Acute Pulmonary Embolism ◽  
Verrucous Carcinoma ◽  
Psoriasis Patient ◽  
Large Tumor ◽  
Embolie Pulmonaire ◽  
Drug Ingestion ◽  
Arsenic Ingestion ◽  
The Right

Background and Objective: Verrucous carcinoma is a rare clinicopathologic entity caused by multifactorial influences. We report here a 64-year-old male patient presenting with a large exophytic mass in the right leg. Results and Conclusion: The patient had a 19-year duration of psoriasis and received various treatments. In his last year of life, he had been taking an illegally produced folk drug with the hope of controlling his psoriasis. However, 6 months after the drug ingestion, many papules appeared on his right leg, which eventually developed into a large tumor in the next few months. The patient died of acute pulmonary embolism only a week after hospitalization, when his tumor was pathologically confirmed as verrucous carcinoma. Later, the folk drug was analyzed and found to contain arsenic. The causative relevance of the tumor with his daily arsenic intake is discussed. Contexte et objectif: Le carcinome verruqueux est une entité clinicopathologique rare, causée par divers facteurs. Nous exposons ici le cas d'un homme de 64 ans, qui a consulté pour une grosse masse exophytique sur la jambe droite. Résultats et conclusions: Le patient souffrait de psoriasis depuis 19 ans et a été soumis à divers traitements. Au cours de sa dernière année de vie, il a pris un remède empirique traditionnel, illégal, dans l'espoir de soulager le psoriasis. Cependant, 6 mois après la consommation du remède, de nombreuses papules sont apparues sur la jambe droite, et ont fini par former une grosse tumeur au cours des mois suivants. Le patient est mort d'une embolie pulmonaire aiguë, une semaine seulement après son hospitalisation, lorsque l'examen histopathologique de la tumeur a révélé qu'il s'agissait d'un carcinome verruqueux. Le remède a été analysé plus tard, et il s'est avéré que celui-ci contenait de l'arsenic. Le lien de cause à effet entre la tumeur et la consommation quotidienne d'arsenic fera l'objet de discussion.

scholarly journals A Case of Proliferative Myositis Arising from the Sternocleidomastoid Muscles: Diagnosis and Treatment

2020 ◽  
Vol 63 (11) ◽  
pp. 537-540
Author(s):  
Bo Hae Kim ◽  
Wook Jang ◽  
Sang Woo Kim ◽  
Woo-jin Jeong
Keyword(s):  
Computed Tomography ◽  
Core Needle Biopsy ◽  
Needle Biopsy ◽  
Treatment Process ◽  
Surgical Excision ◽  
Sternocleidomastoid Muscle ◽  
Diagnosis And Treatment ◽  
Core Needle ◽  
The Right ◽  
Proliferative Myositis

We describe here diagnosis treatment of a case that rose from the sternocleidomastoid muscle and was treated without surgical excision. A 56-year-old man presented with a rapidly growing, painless and not well-circumscribed mass at the right side of the neck. We diagnosed this tumor as proliferative myositis (PM) based on the typical findings from ultrasonography, computed tomography, and core-needle biopsy, and treated it without surgical excision. Herein we report a successful diagnosis and treatment process of a case of PM, which was followed-up with ultrasonography.

Hepatic brucelloma: a rare complication of a common zoonotic disease

2020 ◽  
Vol 13 (12) ◽  
pp. e237076
Author(s):  
George Vatidis ◽  
Eirini I Rigopoulou ◽  
Konstantinos Tepetes ◽  
George N Dalekos
Keyword(s):  
Rare Complication ◽  
Surgical Excision ◽  
Coombs Test ◽  
Inflammation Markers ◽  
Laboratory Findings ◽  
Ct Guided ◽  
Rare Manifestation ◽  
Bone Marrow Cultures ◽  
History Of ◽  
The Right

Hepatic brucelloma (HB), a rare manifestation of brucellosis, refers to liver involvement in the form of abscess. A 35-year-old woman stockbreeder was admitted due to 1-month history of evening fever, sweating and weight loss, while she was on 3-week course of rifampicin/doxycycline for suspected brucellosis. On admission, she had hepatosplenomegaly and a systolic murmur, while cholestasis, increased inflammation markers and a strong-positive Wright-Coombs test were the main laboratory findings. As blood and bone marrow cultures were unrevealing, further investigation with CT imaging showed a central liver calcification surrounded by heterogeneous hypodense area being compatible with HB. Material from CT-guided drainage tested negative for Brucella spp. After failure to improve on a 10-week triple regiment, surgical excision was decided and Brucella spp were identified by PCR. Our case highlights challenges in establishing HB diagnosis, which should be considered on the right epidemiological context and when serological and radiological evidence favour its diagnosis.

scholarly journals Intrascrotal lipoblastoma in adulthood

2019 ◽  
Vol 12 (12) ◽  
pp. e231320
Author(s):  
Mário José Pereira-Lourenço ◽  
Duarte Vieira-Brito ◽  
João Pedro Peralta ◽  
Noémia Castelo-Branco
Keyword(s):  
Case Report ◽  
Magnetic Resonance ◽  
S100 Protein ◽  
Surgical Excision ◽  
Large Mass ◽  
Histological Diagnosis ◽  
Physical Exam ◽  
Nodular Lesion ◽  
Inferior Portion ◽  
The Right

This case report describes the case of a 37-year-old man that noticed an intrascrotal right mass with 1 month of evolution. During physical exam presented with a large mass at the inferior portion of the right testicle, clearly separated from the testicle, with a tender consistency and mobile. An ultrasound was performed that showed a solid and subcutaneous nodular lesion, extra testicular, heterogeneous, measuring 7.2 cm. Pelvic magnetic resonance imageMRI showed a lesion compatible with a lipoma. The patient was subjected to surgical excision of the lesion by scrotal access, having histology revealed a lipoblastoma (LB) of the scrotum. Histological diagnosis was obtained by microscopic characteristics (well-circumscribed fatty neoplasm) and immunohistochemistry (stains for CD34, S100 protein and PLAG1 were positive; stains for MDM2 and CDK4 were negative). LB is extremely rare after adolescence in any location, being this first described case of intrascrotal LB described in adulthood.

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