scholarly journals Juvenile Hyaline Fibromatosis: Literature Review and a Case Treated With Surgical Excision and Corticosteroid

Cureus ◽  
2020 ◽  
Author(s):  
Omar Braizat ◽  
Saif Badran ◽  
Atalla Hammouda
Keyword(s):  
Literature Review ◽  
Surgical Excision ◽  
Juvenile Hyaline Fibromatosis

scholarly journals Endometriosis of Rectus Muscle Excised During Cesarean Section: A Case Report and Literature Review

2016 ◽  
Author(s):  
Recep Erin ◽  
Kübra Baki Erin ◽  
Derya Burkankulu Ağırbaş ◽  
Burcu Kemal Okatan
Keyword(s):  
Case Report ◽  
Pregnant Woman ◽  
Literature Review ◽  
Cesarean Section ◽  
Abdominal Wall ◽  
Rectus Muscle ◽  
Surgical Excision ◽  
Treatment Method ◽  
Abdominal Wall Endometriosis ◽  
Subcutaneous Mass

<p>We aimed to present a case with abdominal wall endometriosis following cesarean section in this case report. <br />A 32 year old 39 weeks pregnant woman with G2P1 was admitted to gynaecology clinic with abdominal lump and pain in the midline. Her physical examination included a hard and painful palpable subcutaneous mass of 4x5 cm size in the midline of the abdomen which was semisolid and irreducible. <br />Under general anesthesia, the mass on the rectus muscle was excised with the healthy tissue around with the diagnosis of endometriosis during cesarean section and the pathological diagnosis was reported as endometriosis.<br />Surgical excision is the best treatment method in abdominal wall endometriosis. <br /><br /></p>

scholarly journals Juvenile hyaline fibromatosis: a rare oral disease case report and literature review

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Liang Xia ◽  
Yuhua Hu ◽  
Chunye Zhang ◽  
Dandan Wu ◽  
Yang Chen
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Oral Disease ◽  
Disease Case ◽  
Juvenile Hyaline Fibromatosis

Laryngeal Langerhans Cell Histiocytosis: A Case Report and Literature Review

2020 ◽  
pp. 000348942095488
Author(s):  
Allen S. Zhou ◽  
Lei Li ◽  
Thomas L. Carroll
Keyword(s):  
Literature Review ◽  
Langerhans Cell Histiocytosis ◽  
Medical Center ◽  
Tertiary Care ◽  
Rare Condition ◽  
Surgical Excision ◽  
Langerhans Cell ◽  
Histopathological Analysis ◽  
Current Case ◽  
Tertiary Care Medical Center

Objective: To describe a case of laryngeal Langerhans cell histiocytosis, discuss its characteristic features and management, and provide a review of the available literature. Methods: A patient presenting to a tertiary care medical center with dyspnea and hoarseness is described. A literature review of laryngeal Langerhans cell histiocytosis cases was performed through a search of articles indexed in the National Institutes of Health PubMed system. Results: We report a case of a 69-year old male, who presented with a laryngeal mass highly suspicious for laryngeal squamous cell carcinoma, was treated with laser excision, and was subsequently found to have laryngeal Langerhans cell histiocytosis upon histological analysis. Including our current case, we found six prior reported cases of laryngeal Langerhans cell histiocytosis in the literature. Of the six cases, four were in adults, while two were in children. Dyspnea is a common presenting complaint present in all cases. Smoking may be a potential risk factor. Conclusions: Laryngeal Langerhans cell histiocytosis is a rare condition and an important consideration in the differential diagnosis of patients presenting with a laryngeal mass and symptoms of dyspnea or hoarseness. Biopsy and histopathological analysis are key to the diagnosis. Surgical excision and radiotherapy are successful treatments used in clinical practice.

Juvenile hyaline fibromatosis: A report of two unrelated adult sibling cases and a literature review

1998 ◽  
Vol 48 (3) ◽  
pp. 230-236 ◽  
Author(s):  
Hideto Senzaki ◽  
Yasuhiko Kiyozuka ◽  
Yoshiko Uemura ◽  
Nobuaki Shikata ◽  
Satoshi Ueda ◽  
...  
Keyword(s):  
Literature Review ◽  
Adult Sibling ◽  
Juvenile Hyaline Fibromatosis ◽  
Unrelated Adult ◽  
Sibling Cases

Dermoid Cyst of the Lateral Neck: A Case Report and Literature Review

1998 ◽  
Vol 77 (2) ◽  
pp. 125-132 ◽  
Author(s):  
David Rosen ◽  
Ari Wirtschafter ◽  
Vijay M. Rao ◽  
Thomas O. Wilcox
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Head And Neck ◽  
Dermoid Cyst ◽  
Surgical Excision ◽  
Lateral Neck ◽  
Fluid Level

Dermoid cysts of the lateral neck are rare, with the majority of head and neck dermoids occurring in the midline. The demonstration of a fat-fluid level on MRI or CT is diagnostic for a cervical dermoid cyst. The treatment of choice remains surgical excision.

Accessory Calcaneus: A Case Report and Literature Review

1995 ◽  
Vol 16 (10) ◽  
pp. 646-650 ◽  
Author(s):  
John O. Krause ◽  
Andrew M. Rouse
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Range Of Motion ◽  
Subtalar Joint ◽  
Surgical Excision ◽  
Degenerative Changes ◽  
Lateral Aspect ◽  
Accessory Ossicles ◽  
Accessory Ossicle

A case of bilateral accessory calcanii is presented in which the accessory ossicle articulated with the talus and calcaneus at the lateral aspect of the posterior facet of the subtalar joint, causing premature subtalar degenerative changes in a 19-year-old man. Although rare and usually asymptomatic, accessory ossicles around the foot may need surgical excision if painful or if sufficient size is obtained to cause deformity and/or limitations in range of motion.

Nasal haemangiopericytoma: report of two cases with literature review

1999 ◽  
Vol 113 (3) ◽  
pp. 199-206 ◽  
Author(s):  
Rémi Marianowski ◽  
Michel Wassef ◽  
Philippe Herman ◽  
Partice Tran Ba Huy
Keyword(s):  
Local Recurrence ◽  
Literature Review ◽  
Paranasal Sinuses ◽  
Surgical Excision ◽  
Lateral Rhinotomy ◽  
Vascular Tumour ◽  
Wide Surgical Excision ◽  
Incomplete Removal ◽  
Midfacial Degloving

AbstractHaemangiopericytoma (HPC) is a rare vascular tumour produced by proliferation of pericytes. One hundred and thirty-three cases of HPC have been reported in the nose and the paranasal sinuses. We present two more cases. Wide surgical excision via lateral rhinotomy, midfacial degloving, or endonasal removal is the treatment of choice. Radiotherapy has been used post-operatively in cases of incomplete removal. Life-long follow-up is required to evaluate local recurrence and late metastases.

Mucosal melanoma arising in the eustachian tube

2006 ◽  
Vol 120 (3) ◽  
pp. 1-3 ◽  
Author(s):  
Seung Jae Baek ◽  
Mee Hyun Song ◽  
Beum Jin Lim ◽  
Won Sang Lee
Keyword(s):  
Literature Review ◽  
Eustachian Tube ◽  
Adjuvant Radiotherapy ◽  
Systemic Chemotherapy ◽  
Neck Region ◽  
Surgical Excision ◽  
Mucosal Melanoma ◽  
Complete Excision ◽  
Head And Neck Region ◽  
Mass Size

Mucosal melanoma is a very rare disease. Most cases have their origins in the head and neck region. To date, only three cases of melanoma originating from the eustachian tube have been reported. We present a case of mucosal melanoma of eustachian tube origin in which a complete excision was performed. In this case, the patient underwent adjuvant radiotherapy and the mass size greatly decreased, which aided subsequent surgical excision. Systemic chemotherapy was not utilized in this case; however, it is often used for palliative purposes. A literature review is also presented.

scholarly journals Peritoneal Pseudocyst Causing Acute Abdomen as a Complication of Cronh’s Disease

2021 ◽  
Vol 64 (1) ◽  
pp. 55-59
Author(s):  
Christos Damaskos ◽  
Nikolaos Garmpis ◽  
Anna Garmpi ◽  
Aliki Liakea ◽  
Dimitrios Mantas
Keyword(s):  
Peritoneal Dialysis ◽  
Literature Review ◽  
Acute Abdomen ◽  
Continuous Ambulatory Peritoneal Dialysis ◽  
Treatment Option ◽  
Surgical Excision ◽  
Emergency Laparotomy ◽  
Postoperative Results ◽  
Therapeutic Problem ◽  
Variable Presentation

Peritoneal pseudocysts (PPs) in patients who are diagnosed with Crohn’s disease (CD), is a rarely diagnosed entity with unknown epidemiology, etiology and pathogenesis. We present the case of a 30-year old male with known CD who presented with an acute abdomen because of a PP. PPs are developed as a complication caused in patients, suffering from mainly thee conditions. Firstly, PPs appear in patients with continuous ambulatory peritoneal dialysis (CAPD), they are also developed in patients with peritoneal trauma and finally in CD patients. Our case belongs to these three reported cases in our literature review, since it refers to a CD patient that developed PPs. He underwent emergency laparotomy and excision of the cyst, with good postoperative results. A literature review of 22 publications show that PPs often represent a diagnostic and therapeutic problem as it has a variable presentation and there are no data on what the best treatment option is – surgical excision or aspiration.

scholarly journals Illustration by Two Cases of the Treatment of Axillary Verneuil Disease with a TDAP Flap

2020 ◽  
pp. 1-4
Author(s):  
Mohamed Raboune ◽  
A. Abbassi ◽  
I. Moqfi ◽  
J. Hafidi ◽  
Mohamed Raboune ◽  
...  
Keyword(s):  
Literature Review ◽  
Perforator Flap ◽  
Surgical Excision ◽  
Therapeutic Options ◽  
Aesthetic Outcome ◽  
Verneuil’S Disease ◽  
Axillary Region ◽  
Tdap Flap ◽  
Verneuil Disease

In this article, we have described two cases of Verneuil’s disease (H.S) which benefited from radical surgical excision, and followed by reconstruction of the axillary region with a TDAP perforator flap, and we carried out a literature review to highlight the interest of this technique and compare it with other therapeutic options in terms of complications, and also the functional and aesthetic outcome.

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