scholarly journals Gardner’s syndrome (literature review and case report)

2020 ◽  
Vol 10 (2) ◽  
pp. 47-52
Author(s):  
I. L. Chernikovskiy ◽  
D. N. Korobkov ◽  
N. V. Savanovich ◽  
D. A. Chernikov ◽  
P. V. Melnikov ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Literature Review ◽  
Soft Tissue Tumors ◽  
Gardner's Syndrome ◽  
Gardner’S Syndrome ◽  
Treatment Methods ◽  
Disease Epidemiology ◽  
Genetically Determined

Gardner’s syndrome is a genetically determined disease characterized by a combination of colon polyposis, osteomas, and various soft tissue tumors. In this article, we discuss disease epidemiology, etiology, manifestations, and treatment methods. We also report a case of Gardner’s syndrome.

Turcot syndrome and Gardner's syndrome in a female patient with familial colon adenomatosis. A case report and literature review

2019 ◽  
Vol 83 (6) ◽  
pp. 72
Author(s):  
A. M. Kuz'minov ◽  
D. V. Vyshegorodtsev ◽  
M. Kh. Toboeva ◽  
V. Yu. Korolik ◽  
A. V. Gavryushin ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Female Patient ◽  
Gardner's Syndrome ◽  
Gardner’S Syndrome ◽  
Turcot Syndrome

scholarly journals Extracalvarial Composite Infantile Myofibromatosis: Case Report and Literature Review

2016 ◽  
Vol 04 (01) ◽  
pp. 022-025 ◽  
Author(s):  
Alexander Ivanov ◽  
Tibor Valyi-Nagy ◽  
Dimitrios Nikas
Keyword(s):  
Case Report ◽  
Genetic Testing ◽  
Soft Tissue ◽  
Literature Review ◽  
Clinical Course ◽  
Treatment Options ◽  
Soft Tissue Tumors ◽  
Infantile Myofibromatosis ◽  
Histopathological Features

Infantile soft tissue tumors of the head are very rare and the majority of them are myofibromas. The authors present the case of a 1-day-old boy with a scalp tumor with several distinct histopathological features including myofibroma, hemangiopericytoma, and fibrosarcoma consistent with the diagnosis of composite infantile myofibromatosis. Genetic testing was negative for trisomy 17, translocation (12; 15), FUS, and ETV6 translocations. Despite the ominous histopathological features, the clinical course was benign. The authors review here available literature concerning current concepts of making the diagnosis of composite infantile myofibromatosis and discuss treatment options.

scholarly journals A Case of Early FAP Diagnosis with Extraintestinal Manifestations on the Face

2019 ◽  
Vol 48 (2) ◽  
pp. 217
Author(s):  
Vasilios Thomaidis ◽  
Konstantinos Seretis ◽  
Gregory Tsoucalas ◽  
Konstantinos Razos ◽  
Anastasios Vasilopoulos ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Clinical Signs ◽  
Gardner's Syndrome ◽  
Colon Polyps ◽  
Extraintestinal Manifestations ◽  
Adenomatous Polyposis ◽  
Gardner’S Syndrome ◽  
Soft Tissue Lesions ◽  
The Face

<p><strong>Objective. </strong>Gardner’s syndrome is a variant of familial adenomatous polyposis, characterized by gastrointestinal polyps, multiple osteomas, and skin and soft tissue lesions. Diagnosis by means of an understanding of its various symptoms is of great importance.</p><p><strong>Case report. </strong>This report presents the case of a 32-year-old man with obvious asymmetry and disfigurement on his face, due to multiple osteomas and soft tissue lesions. These clinical signs prompted us to further investigation, leading to the diagnosis of a case of Gardner’s syndrome, with asymptomatic polyposis of the colon. Polyps have virtually an almost 100% risk of undergoing malignant transformation.</p><p><strong>Conclusion. </strong>Early diagnosis and treatment of this pathological entity are crucial, while the presence of osteomas should alert us to this diagnosis.</p>

scholarly journals Desmoid tumor of the foot: a case report and literature review

2021 ◽  
pp. 17
Author(s):  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Literature Review ◽  
Desmoid Tumor ◽  
Soft Tissue Tumors ◽  
Review Of The Literature ◽  
Rare Tumors

A desmoid tumor (DT) was first described by MacFarlane in 1832. DTs are rare tumors, corresponding to only 0.03% of all neoplasia and less than 3% of all soft tissue tumors. Most of the tumors occur in the abdomen and presentation in the extremities is uncommon. Here, we present a review of the literature and the 27th case of DT of the foot.

scholarly journals Bone and dental abnormalities as first signs of familial Gardner’s syndrome in a Chinese family: a literature review and a case report

2018 ◽  
Vol 34 ◽  
pp. 20-25 ◽  
Author(s):  
Dan Yu ◽  
Benjamin NG CW ◽  
Huiyong Zhu ◽  
Jianhua Liu ◽  
Yi Lin
Keyword(s):  
Gastrointestinal Symptoms ◽  
Soft Tissue Tumors ◽  
Chinese Family ◽  
Gardner's Syndrome ◽  
Dental Anomalies ◽  
Gardner’S Syndrome ◽  
Intestinal Polyps ◽  
Family Pedigree ◽  
Caucasian Race ◽  
Dominant Disease

Gardner’s syndrome (GS) is an autosomal dominant disease characterized by the presence of familial adenomatous polyposis (FAP) as well as extraintestinal manifestations such as osteomas, dental anomalies, epidermoid cysts and ocular abnormalities. These intestinal polyps carry a 100% risk of malignant change, so early diagnosis is crucial. As craniofacial osteomas and dental anomalies of GS usually precede gastrointestinal symptoms, otolaryngologists, oral surgeons and dentists play an important role in the diagnosis of GS. GS is extensively reported in literature in the Caucasian race but not in the Mongoloid race. We report a case of a 22-year-old patient with a manifestation of three features of GS - multiple osteomas, soft tissue tumors and dental anomalies in the craniofacial region, with no intestinal polyps at the time of reporting. A family pedigree with our patient as the proband was constructed and revealed 3 consecutive generations in his lineage with GS.

scholarly journals Male urethral sarcoma: a case report and literature review

2015 ◽  
Vol 14 (1) ◽  
pp. 64-66
Author(s):  
Magno Almeida Nogueira ◽  
Guilherme Campelo Lopes dos Santos ◽  
Roberto Iglesias Lopes ◽  
Octavio Henrique Arcos Campos ◽  
Marcos Francisco Dall'Oglio ◽  
...  
Keyword(s):  
Case Report ◽  
Urinary Tract ◽  
Soft Tissue ◽  
Literature Review ◽  
Soft Tissue Sarcomas ◽  
Heterogeneous Group ◽  
Men 2

Urethral tumors are rare and aggressive. They usually affect men (2:1) and occur more commonly in white (85% of cases). Soft tissue sarcomas are a heterogeneous group of tumors that arise from embryonic mesoderm. It represents 1% of all cases of urinary tract malignancies and rarely primary affect the ureter. We report a case of male urethral sarcoma. To date, only two similar cases have been published in literature.

scholarly journals Bifocal parosteal osteoma of femur: A case report and review of literature

2020 ◽  
Author(s):  
Raffaele Vitiello ◽  
Tommaso Greco ◽  
Luigi Cianni ◽  
Silvia Careri ◽  
Maria Serena Oliva ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Features ◽  
Compact Bone ◽  
Gardner's Syndrome ◽  
Review Of Literature ◽  
Solitary Lesion ◽  
Gardner’S Syndrome ◽  
One Year

Osteoma is a benign, slowly growing, asymptomatic, bone-forming tumor arising from cancellous or compact bone. Osteoma usually is a solitary lesion, but in patients with Gardner’s Syndrome it may be multiple. osteoma may rarely have a parosteal localization. Parosteal osteoma has peculiar radiographic, histologic and clinical features. We describe a case report of a 51- years old man with a bifocal parosteal osteoma of the femur in a non-syndromic patient. This is the first described patient with a bifocal lesion. In literature only 24 cases of paraosteal osteoma are found. Our patient underwent surgery and the lesions were fully excised. At one year follow-up there was no evidence of recurrence.

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