Natal maxillary primary molars: case report

An unusual case of a newborn with two immature natal maxillary molars is presented. Clinical and histological examination showed that the teeth were rootless and incompletely mineralized. The patient was followed up during one year and we confirmed that the natal teeth were from normal primary series.

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Large solitary neurofibroma of the cheek mucosa: a case report

Research Society and Development ◽

10.33448/rsd-v10i2.12905 ◽

2021 ◽

Vol 10 (2) ◽

pp. e56810212905

Author(s):

Andre Luis Costa Cantanhede ◽

Carolinne da Gloria Araújo ◽

Priscila Mayara Silva de Almeida ◽

Hassan Lavalier de Oliveira Lima

Keyword(s):

Case Report ◽

Oral Cavity ◽

Schwann Cells ◽

Histological Examination ◽

Unusual Case ◽

Surgical Excision ◽

Benign Tumors ◽

Intraoral Approach ◽

S 100 ◽

Neural Origin

Neurofibromas are uncommon benign tumors in the oral cavity, which are composed of Schwann cells, perineural-like cells, and fibroblasts. The diagnosis can be confirmed by histological examination and immunopositivity for the S-100 protein indicating its neural origin. Surgical excision is the treatment of choice, and the intraoral approach is the best route for a medium-sized lesion and the prognosis is excellent. This paper aims at to present a unusual case of large neurofibroma located at the cheek mucosa of a young man and review important aspects of this tumor in the oral cavity.

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Dysphagia Induced by Nasal Septal Chondroma: A Case Report

Journal of Nepal Medical Association ◽

10.31729/jnma.3953 ◽

2019 ◽

Vol 57 (217) ◽

Author(s):

Seog-Kyun Mun ◽

Hyun-kyu Chae ◽

Mun-Young Chang ◽

Seog-Kyun Mun

Keyword(s):

Case Report ◽

Nasal Septum ◽

Normal Tissue ◽

Unusual Case ◽

Endoscopic Removal ◽

One Year

Chondromas rarely occur in the nasal area and are usually found in the metaphyseal area of thephalanges and metacarpals of the hands, as well as the pelvis, sternum and scapula. The authorspresent an unusual case of dysphagia induced by histologically confirmed chondroma arising fromthe nasal septum. Treatment is to completely remove the mass with adequate margins of normaltissues to prevent recurrence and malignancy. Intranasal endoscopic removal of tumor with anadequate margin of normal tissue. After one year of treatment, there was no evidence of recurrence.We present a case of nasal septal chondroma in 18 year male.

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Hemangiomatosis of the greater omentum – a case report

Perspectives in Surgery ◽

10.33699/pis.2019.98.4.178-180 ◽

2019 ◽

Vol 98 (4) ◽

pp. 178-180

Keyword(s):

Case Report ◽

Surgical Treatment ◽

Histological Examination ◽

Case Reports ◽

Greater Omentum ◽

Surgical Removal ◽

Consumption Coagulopathy ◽

Cavernous Hemangiomas ◽

Mesodermal Origin ◽

Benign Tumours

Cavernous hemangiomas are benign tumours of mesodermal origin. Even though various localizations of hemangioma have been described in the literature, its occurrence in the greater omentum is very rare. Only symptomatic hemangiomas are indicated for surgical treatment. There are case reports presenting resection or surgical removal of the greater omentum with hemangioma because of mechanical syndrome, consumption coagulopathy, bleeding, infection or suspicion of a malignancy. This article presents a case report of a patient operated on for a suspicion of carcinomatosis of the greater omentum. Histological examination found hemangiomatosis in the resected greater omentum.

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Chylopericardium following Atrial Septal Defect Repair: Case Report

The Heart Surgery Forum ◽

10.1532/hsf98.20041118 ◽

2005 ◽

Vol 8 (1) ◽

pp. 23 ◽

Cited By ~ 2

Author(s):

Sanjay Kumar ◽

Bharati Sinha

Keyword(s):

Case Report ◽

Atrial Septal Defect ◽

Cardiac Tamponade ◽

Unusual Case ◽

Septal Defect ◽

Clinical Course ◽

Defect Repair ◽

Cardiac Operations

Chylopericardium after intrapericardial cardiac operations is extremely rare. We present an unusual case of postoperative chylopericardium with cardiac tamponade following atrial septal defect repair, and we comment on the clinical course and treatment.

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Case Report: An Unusual Case of systemic Hydatid Disease

Indian Journal Of Applied Research ◽

10.15373/2249555x/july2014/187 ◽

2011 ◽

Vol 4 (7) ◽

pp. 537-538

Author(s):

Dr. Saurabh Chaudhuri ◽

◽

Dr. Priscilla Joshi ◽

Dr. Mohit Goel ◽

Dr. Wasim Siddiqui

Keyword(s):

Case Report ◽

Hydatid Disease ◽

Unusual Case

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Premalignant and Malignant Lesions of the Heterotopic Pancreas in the Esophagus: a Case Report and Review of the Literature

Journal of Gastrointestinal and Liver Diseases ◽

10.15403/jgld.2014.1121.242.uly ◽

2015 ◽

Vol 24 (2) ◽

pp. 235-239 ◽

Cited By ~ 9

Author(s):

Jan Ulrych ◽

Vladimir Fryba ◽

Helena Skalova ◽

Zdenek Krska ◽

Tomas Krechler ◽

...

Keyword(s):

Case Report ◽

Gastrointestinal Tract ◽

Unusual Case ◽

Accurate Diagnosis ◽

Heterotopic Pancreas ◽

Premalignant Lesions ◽

Resected Specimen ◽

Review Of The Literature ◽

Severe Dysphagia ◽

Malignant Lesions

Heterotopic pancreas is a congenital pathology of the gastrointestinal tract, particularly rare in the esophagus. Both symptomatology and findings during preoperative examinations are non-specific and therefore do not often lead to an accurate diagnosis, which is usually revealed only by histopathological assessment of a resected specimen. We report an unusual case of a patient suffering from severe dysphagia caused by heterotopic pancreas in the distal esophagus with chronic inflammation and foci of premalignant changes. This article also reviews 14 adult cases of heterotopic pancreas in the esophagus previously reported in the literature, with the aim of determining the clinical features of this disease and possible complications including rare premalignant lesions and malignant transformation. Especially with regard to those complications, we suggest that both symptomatic and incidentally found asymptomatic lesions should be resected.

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