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Items 1 to 54 of about 54
1. Diniz MB, Giro Elisa MA, Zuanon Angela CC, Costa CA, Hebling J: Congenital epulis: a rare benign tumor in the newborn. J Indian Soc Pedod Prev Dent; 2010 Jul-Sep;28(3):230-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital epulis: a rare benign tumor in the newborn.
  • Congenital epulis (CE) of the newborn is a rare benign soft tissue tumor that presents at birth.
  • The lesion is more common in female neonates and normally affects the maxillary alveolar ridge.
  • A decisive diagnosis is made by histopathologic analysis as other newborn lesions can be incorrectly diagnosed as CE.
  • This article presents a case report of a female infant who presented a fibrotic mass in the primary lateral incisor and canine region of the maxillary alveolar ridge.
  • [MeSH-major] Gingival Neoplasms / congenital. Gingival Neoplasms / pathology

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  • (PMID = 21157060.001).
  • [ISSN] 0970-4388
  • [Journal-full-title] Journal of the Indian Society of Pedodontics and Preventive Dentistry
  • [ISO-abbreviation] J Indian Soc Pedod Prev Dent
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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2. Jang SI, Lee EJ, Hart PS, Ramaswami M, Pallos D, Hart TC: Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosis. J Biol Chem; 2007 Jul 13;282(28):20245-55
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosis.
  • Mutation of human SOS1 is responsible for hereditary gingival fibromatosis type 1, a benign overgrowth condition of the gingiva.
  • Here, we investigated molecular mechanisms responsible for the increased rate of cell proliferation in gingival fibroblasts caused by mutant SOS1 in vitro.
  • Additionally, we observed an increase in the magnitude and duration of ERK signaling in hereditary gingival fibromatosis gingival fibroblasts that was associated with phosphorylation of retinoblastoma tumor suppressor protein and the up-regulation of cell cycle regulators, including cyclins C, D, and E and the E2F/DP transcription factors.
  • These factors promote cell cycle progression from G(1) to S phase, and their up-regulation may underlie the increased gingival fibroblast proliferation observed.
  • These findings elucidate the mechanisms for gingival overgrowth mediated by SOS1 gene mutation in humans.
  • [MeSH-major] Fibroblasts / metabolism. Fibromatosis, Gingival / metabolism. G1 Phase. MAP Kinase Signaling System. S Phase. SOS1 Protein / metabolism

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  • (PMID = 17510059.001).
  • [ISSN] 0021-9258
  • [Journal-full-title] The Journal of biological chemistry
  • [ISO-abbreviation] J. Biol. Chem.
  • [Language] eng
  • [Grant] United States / Intramural NIH HHS / /
  • [Publication-type] Journal Article; Research Support, N.I.H., Intramural
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Cyclins; 0 / E2F Transcription Factors; 0 / EGR1 protein, human; 0 / Early Growth Response Protein 1; 0 / Proliferating Cell Nuclear Antigen; 0 / RNA, Small Interfering; 0 / Retinoblastoma Protein; 0 / SOS1 Protein; EC 2.7.11.24 / Extracellular Signal-Regulated MAP Kinases
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3. Eguia A, Uribarri A, Gay Escoda C, Crovetto MA, Martínez-Conde R, Aguirre JM: Granular cell tumor: report of 8 intraoral cases. Med Oral Patol Oral Cir Bucal; 2006 Aug;11(5):E425-8
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  • [Title] Granular cell tumor: report of 8 intraoral cases.
  • Granular cell tumor (GCT) is an uncommon neoplasm of controversial origin that can appear in any corporal localization, including the orofacial region.
  • Although aggressive and malignant variants of this neoplasm have been described, most of GCTs are benign.
  • In spite of the amount of research, the etiology of this neoplasm remains unclear and its histogenesis and its possible muscular, connective or neural origin has been broadly debated.
  • The main clinicopathologic and diagnostic features of this neoplasm are reviewed and discussed.
  • [MeSH-major] Granular Cell Tumor / pathology. Mouth Neoplasms / pathology
  • [MeSH-minor] Adolescent. Adult. Female. Gingival Neoplasms / pathology. Humans. Male. Middle Aged. Mouth Mucosa / pathology. Tongue Neoplasms / pathology

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  • (PMID = 16878061.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng; spa
  • [Publication-type] Journal Article
  • [Publication-country] Spain
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4. Abrahão AC, Camisasca DR, Bonelli BR, Cabral MG, Lourenço SQ, Torres SR, Pinto DS Jr: Recurrent bilateral gingival peripheral calcifying epithelial odontogenic tumor (Pindborg tumor): a case report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep;108(3):e66-71
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Recurrent bilateral gingival peripheral calcifying epithelial odontogenic tumor (Pindborg tumor): a case report.
  • Calcifying epithelial odontogenic tumor (CEOT) is an extremely rare, benign neoplasm, accounting for approximately 1% of all odontogenic tumors.
  • A 40-year-old female presented with bilateral soft, painful, erythematous, gingival swellings localized in premolar areas of the mandibular gingiva.
  • The presumptive diagnosis was bilateral pyogenic granuloma.
  • Morphologic features, and histochemical and immunohistochemical tests revealed bilateral peripheral calcifying odontogenic epithelial tumor.
  • Gingival masses must be carefully evaluated for clinical and histologic evidence of neoplasia.
  • [MeSH-major] Gingival Neoplasms / diagnosis. Neoplasm Recurrence, Local / diagnosis. Odontogenic Tumors / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Follow-Up Studies. Gingival Diseases / diagnosis. Granuloma, Pyogenic / diagnosis. Humans. Immunohistochemistry

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  • (PMID = 19716494.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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5. Chatterjee A, Ajmera N, Singh A: Peripheral cemento-ossifying fibroma of maxilla. J Indian Soc Periodontol; 2010 Jul;14(3):186-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Peripheral cemento-ossifying fibroma is a reactive gingival overgrowth occurring frequently in anterior maxilla.
  • It is a slow-growing benign tumor which may lead to pathologic migration and other periodontal problems, so it should be excised as soon as possible.

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  • [Cites] Otolaryngol Head Neck Surg. 2000 May;122(5):775 [10793367.001]
  • [Cites] J Periodontol. 2001 Jul;72(7):939-44 [11495143.001]
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  • (PMID = 21760674.001).
  • [ISSN] 0975-1580
  • [Journal-full-title] Journal of Indian Society of Periodontology
  • [ISO-abbreviation] J Indian Soc Periodontol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3100863
  • [Keywords] NOTNLM ; Fibroma / gingival overgrowth / peripheral cemento-ossifying fibroma
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6. Curien R, Moizan H, Gerard E: Gingival metastasis of a bronchogenic adenocarcinoma: report of a case. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 Dec;104(6):e25-8
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  • [Title] Gingival metastasis of a bronchogenic adenocarcinoma: report of a case.
  • We report the case of a 64-year-old patient suffering from a multiple metastatic bronchial adenocarcinoma, referred to our department for a gingival tumefaction.
  • The diagnostic assumptions considered were those of a pyogenic granuloma, of a primary gingival carcinoma, or of a metastasis of the bronchial tumor.
  • An excisional biopsy was carried out and the histopathologic examination confirmed the latter diagnosis.
  • If metastases of pulmonary cancers represent the majority of gingival metastases, those of bronchial adenocarcinoma are very rare.
  • The main clinical diagnostic difficulty is the distinction between benign lesion and malignant lesion, and between primary lesion and metastasis.
  • Even if gingival metastases are rare, their semiological value incites the histopathologic examination of any presumedly benign tumor of the gingiva.
  • [MeSH-major] Carcinoma, Bronchogenic / secondary. Gingival Neoplasms / secondary. Lung Neoplasms
  • [MeSH-minor] Diagnosis, Differential. Humans. Middle Aged

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  • (PMID = 17942337.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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7. Habibi A, Saghravanian N, Zare R, Jafarzadeh H: Clear cell variant of extraosseous calcifying epithelial odontogenic tumor: a case report. J Oral Sci; 2009 Sep;51(3):485-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clear cell variant of extraosseous calcifying epithelial odontogenic tumor: a case report.
  • Calcifying epithelial odontogenic tumor (CEOT) is a benign epithelial odontogenic tumor occurring most frequently in the posterior part of the lower jaw.
  • Extraosseous CEOT is one of the rarest forms of this tumor, and few such cases involving the maxillary gingiva have been reported in the literature.
  • Here we present a case that showed progressive enlargement in the left maxillary gingival area over a period of 11 years.
  • Histologically, the tumor showed proliferation of sheets and cords of epithelial cells with granular, eosinophilic cytoplasm and round to oval nuclei.
  • The present case of extraosseous CEOT with clear cells was considered to be a very rare form of this tumor.
  • [MeSH-major] Gingival Neoplasms / pathology. Odontogenic Tumors / pathology

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  • (PMID = 19776521.001).
  • [ISSN] 1880-4926
  • [Journal-full-title] Journal of oral science
  • [ISO-abbreviation] J Oral Sci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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8. Bernabé DG, Veronese LA, Miyahara GI, Conrado-Neto S, Biasoli ER: Gingival metastasis from salivary duct carcinoma of the parotid gland. J Periodontol; 2008 Apr;79(4):748-52

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Gingival metastasis from salivary duct carcinoma of the parotid gland.
  • BACKGROUND: This article reports a rare case of metastasis of salivary duct carcinoma of the parotid gland to the gingiva and reviews the occurrence of metastatic processes to the oral mucosa.
  • METHODS: A 67-year-old white male presented with a chief complaint of a painless nodular tissue growth on the gingiva with reportedly 5 months of evolution.
  • The intraoral examination revealed a reddish, superficially ulcerated nodular lesion ( approximately 2 cm in diameter) on the right mandibular buccal attached gingiva, and the clinical aspect was that of a benign reactive lesion.
  • The patient had undergone a parotidectomy for removal of a salivary duct carcinoma of the parotid gland almost 1 year before.
  • A biopsy of the gingival lesion was performed, and the biopsied tissue was forwarded for histopathologic examination.
  • RESULTS: The analysis of the histopathologic sections of the gingival lesion revealed histomorphologic characteristics very similar to those of the primary parotid gland tumor.
  • The definitive diagnosis was gingival metastasis from a salivary duct carcinoma of the parotid gland.
  • The patient died of complications of a pulmonary metastasis 1 month after the diagnosis of the oral metastatic lesion.
  • CONCLUSIONS: Gingival lesions that mimic reactive and hyperplastic lesions may be metastases from malignant neoplasias of diverse origins.
  • An accurate and timely diagnosis is crucial to establish proper and immediate treatment of the metastatic tumor and possibly identify an occult primary malignant neoplasia.
  • [MeSH-major] Carcinoma, Ductal / secondary. Gingival Neoplasms / secondary. Parotid Neoplasms / pathology. Salivary Ducts / pathology

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  • (PMID = 18380570.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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9. Châari C, Hachicha LM, Khoud NB, Ellouze S, Karray F, Abbes K, Abdelmoula M, Krichen SM, Boudawara TS: [A rare congenital gingival tumor]. Ann Pathol; 2009 Dec;29(6):485-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A rare congenital gingival tumor].
  • INTRODUCTION: Congenital epulis (CE) of the newborn also known as congenital granular cell tumor or Neumann tumor is an uncommun benign tumour occuring in the anterior alveolar ridge of the jaws.
  • In our study, we discuss the clinicopathologic and evolutive caracteristics and the diagnosis problems of this entity.
  • OBSERVATION: A newborn girl, two months old, presented at birth a nodular mass in the upper alveolar crete of the maxilla.
  • DISCUSSION: CE is a rare tumor; its etiopathogenesis is still unclear.
  • The diagnosis suspected clinically is confirmed by the histopathological study.
  • [MeSH-major] Gingival Neoplasms / pathology
  • [MeSH-minor] Echocardiography. Fatal Outcome. Female. Genetic Counseling. Homozygote. Humans. Infant. Infant, Newborn. Lung / pathology. Male. Mutation. Polymerase Chain Reaction / methods. Pulmonary Alveolar Proteinosis / genetics. Pulmonary Alveolar Proteinosis / pathology. Pulmonary Alveolar Proteinosis / radiography. Pulmonary Surfactant-Associated Protein B / deficiency. RNA, Messenger / genetics. Radiography, Thoracic

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  • (PMID = 20005436.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Pulmonary Surfactant-Associated Protein B; 0 / RNA, Messenger
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10. Messina M, Severi FM, Buonocore G, Molinaro F, Amato G, Petraglia F: Prenatal diagnosis and multidisciplinary approach to the congenital gingival granular cell tumor. J Pediatr Surg; 2006 Oct;41(10):E35-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prenatal diagnosis and multidisciplinary approach to the congenital gingival granular cell tumor.
  • OBJECTIVE: Congenital gingival granular cell tumor (CGCT) is a rare benign lesion appearing at birth on the alveolar median ridge of the maxilla.
  • Pathology revealed a tumor of large polyedric cells with vacuolar central nuclei and eosinophil granular cytoplasm.
  • CONCLUSIONS: Prenatal diagnosis is fundamental in the therapeutic approach to CGCT: ultrasonography methodologies allow diagnosis of the lesion in the uterus at the 36th gestational week, thus also allowing planning of delivery and, immediately later, the surgical treatment.
  • [MeSH-major] Gingival Neoplasms / surgery. Gingival Neoplasms / ultrasonography. Granular Cell Tumor / surgery. Granular Cell Tumor / ultrasonography. Patient Care Team. Ultrasonography, Prenatal

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  • (PMID = 17011257.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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11. Cheng YS, Kessler H, Rees TD, Philofsky D, Pontikas A: Gingival swelling in a 13-year-old girl with multiple recurrences. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 Jan;103(1):85-91
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  • [Title] Gingival swelling in a 13-year-old girl with multiple recurrences.
  • We present a challenging case of gingival swelling that recurred several times in 3.5 years in a 13-year-old girl.
  • With the tissue specimens from subsequent multiple excisions and several immunohistochemical studies, the diagnoses evolved to benign cellular infiltrate of undetermined origin, epithelioid hemangioma, proliferating endothelial cell neoplasm of uncertain biologic potential, atypical vascular tumor, epithelioid hemangioendothelioma, and kaposiform hemangioendothelioma.
  • We discuss the list of differential diagnoses from various pathologists and propose our diagnosis of epithelioid hemangioendothelioma based on its clinical behavior, histologic features, and immunohistochemical findings.
  • [MeSH-major] Alveolar Process / surgery. Gingiva / pathology. Gingival Neoplasms / pathology. Hemangioendothelioma, Epithelioid / pathology. Neoplasm Recurrence, Local / pathology
  • [MeSH-minor] Adolescent. Angiolymphoid Hyperplasia with Eosinophilia / pathology. Biomarkers / analysis. Biopsy. Diagnosis, Differential. Epithelioid Cells / pathology. Female. Humans. Reoperation

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  • (PMID = 17178499.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers
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12. Farah-Klibi F, Ferchichi L, Beyâa Rassou H, Zairi I, Rameh S, Adouani A, Ben Jilani SB, Zermani R: [Adenomatoid odontogenic tumor: two cases]. Rev Stomatol Chir Maxillofac; 2007 Feb;108(1):61-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Adenomatoid odontogenic tumor: two cases].
  • INTRODUCTION: Adenomatoid odontogenic tumor, initially referred to as adenoameloblastoma, is a rare and benign odontogenic tumor.
  • CASE REPORTS: We report two cases of adenomatoid odontogenic tumor, which illustrate the radiological and anatomic features of this tumor.
  • They occurred in two 21 and 14 years-old teenagers who presented gingival swelling.
  • DISCUSSION: The clinical, radiological and histological features of adenomatoid odontogenic tumor are distinct from those of ameloblastoma.
  • This tumor is frequently misdiagnosed as other odontogenic cysts or tumors.
  • We discuss the anatomoclinical features and the histogenesis of this rare tumor.
  • [MeSH-minor] Adolescent. Adult. Diagnosis, Differential. Female. Humans. Male. Tooth, Impacted / etiology. Tooth, Impacted / surgery

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  • (PMID = 17275864.001).
  • [ISSN] 0035-1768
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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13. Munakata R, Sawair FA, Cheng J, Saku T: Gingival metastasis of ovarian carcinoma: report of a case and review of the literature. Int J Oral Maxillofac Surg; 2009 Oct;38(10):1123-6
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  • [Title] Gingival metastasis of ovarian carcinoma: report of a case and review of the literature.
  • Diagnosing gingival metastases is difficult because clinically they can mimic benign oral lesions.
  • The authors report an unusual case of metastatic ovarian carcinoma in the gingiva of a 46-year-old woman 5 years after ovariectomy.
  • The tumor presented as an exophytic growth at the molar region of the mandible.
  • Tumor cells were immunopositive for carcinoembryonic antigen, MUC1 mucin, and lysozyme, while stromal fibroblasts were immunopositive for vimentin and estrogen receptor.
  • The diagnosis of metastatic ovarian mucinous cystadenocarcinoma was made.
  • A review of the English literature revealed this to be the first report of gingival metastasis of an ovarian carcinoma.
  • [MeSH-major] Cystadenocarcinoma, Mucinous / secondary. Gingival Neoplasms / secondary. Ovarian Neoplasms / pathology

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  • (PMID = 19505797.001).
  • [ISSN] 1399-0020
  • [Journal-full-title] International journal of oral and maxillofacial surgery
  • [ISO-abbreviation] Int J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Carcinoembryonic Antigen; 0 / Mucin-1; 0 / Receptors, Estrogen; 0 / Vimentin
  • [Number-of-references] 27
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14. Scolozzi P, Marret N, Bouzourene H, Luthi F, Bauer J, Jaques B, Lombardi T: Mixed testicular germ cell tumor presenting as metastatic pure choriocarcinoma involving the maxillary gingiva. J Oral Pathol Med; 2006 Oct;35(9):579-81
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  • [Title] Mixed testicular germ cell tumor presenting as metastatic pure choriocarcinoma involving the maxillary gingiva.
  • Gingival metastases are infrequent and invariably associated with a widespread disease and a poor prognosis.
  • Because of their unremarkable clinical appearance, they can be difficult to distinguish from more common gingival hyperplastic or reactive lesions, such as pyogenic granuloma, peripheral giant cell granuloma, and peripheral ossifying granuloma.
  • We are reporting here an unusual case of a 36-year-old man with a mixed testicular germ cell tumor presenting as a metastatic pure choriocarcinoma involving the maxillary gingiva, extending from the first left premolar to the left second maxillary molar, mimicking a 'benign looking' gingival mass.
  • Gingival metastases may be the first manifestation of a widespread metastatic disease and therefore particular attention must be paid to gingival lesions associated with atypical clinical symptoms and/or signs.
  • [MeSH-major] Choriocarcinoma / secondary. Gingival Neoplasms / secondary. Mixed Tumor, Malignant / secondary. Neoplasms, Germ Cell and Embryonal / secondary. Testicular Neoplasms

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  • (PMID = 16968241.001).
  • [ISSN] 0904-2512
  • [Journal-full-title] Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology
  • [ISO-abbreviation] J. Oral Pathol. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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15. Guven S, Kaymakci A, Bugday MS, Yilmaz M: Congenital granular cell tumor. J Craniofac Surg; 2009 May;20(3):976-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital granular cell tumor.
  • Congenital granular cell tumor or congenital epulis is a rare benign soft tissue lesion in newborns.
  • It usually arises from the mucosa of the gingiva, either from the maxillary or mandibular alveolar ridge, and may cause respiratory or feeding problems.
  • We reported a case of a 1-hour-old female newborn with a congenital granular cell tumor in the anterior maxillary alveolar ridge.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital
  • [MeSH-minor] Biomarkers, Tumor / analysis. Cell Nucleus / pathology. Collagen / ultrastructure. Cytoplasm / pathology. Female. Follow-Up Studies. Humans. Infant, Newborn. Maxilla. Phosphopyruvate Hydratase / analysis. Vimentin / analysis

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  • (PMID = 19461349.001).
  • [ISSN] 1536-3732
  • [Journal-full-title] The Journal of craniofacial surgery
  • [ISO-abbreviation] J Craniofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Vimentin; 9007-34-5 / Collagen; EC 4.2.1.11 / Phosphopyruvate Hydratase
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16. Keleş E, Akpolat N, Alpay HC, Tazegül A: [A rare tumor in a newborn: congenital epulis]. Kulak Burun Bogaz Ihtis Derg; 2005;14(3-4):92-5
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  • [Title] [A rare tumor in a newborn: congenital epulis].
  • Physical examination showed a smooth and pedicled mass with normal mucosal tissue, 3x2 cm in size, originating from the maxillary alveolar edge on the upper incisor and canine teeth.
  • Histopathologic diagnosis was congenital epulis.
  • Congenital epulis is a benign tumor.
  • [MeSH-major] Gingival Diseases / diagnosis. Gingival Neoplasms / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Infant, Newborn

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  • (PMID = 16227732.001).
  • [ISSN] 1300-7475
  • [Journal-full-title] Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat
  • [ISO-abbreviation] Kulak Burun Bogaz Ihtis Derg
  • [Language] tur
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Turkey
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17. Abbo O, Breibach F, Vaysse F, Kessler S, Guitard J, Galinier P: [Antenatal diagnosis of a congenital granular cell tumor]. Rev Stomatol Chir Maxillofac; 2010 Apr;111(2):91-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Antenatal diagnosis of a congenital granular cell tumor].
  • [Transliterated title] Tumeur granuleuse gingivale congénitale de découverte anténatale.
  • INTRODUCTION: Neuman's tumors also called congenital epulis or congenital gingival granulomatous tumors are rare and benign oral cavity tumors.
  • A maxillary tumor in the fetus was revealed by the third trimester US.
  • A fetal MRI was prescribed, after discussion with the antenatal diagnostic center, to determine the localization, size, and nature of the tumor.
  • It revealed a 3 cm long tumor with cystic like areas not communicating with the encephalus.
  • Histological analysis confirmed the diagnosis.
  • DISCUSSION: A prenatal diagnosis of congenital gingival granulomatous tumor is rare.
  • Nevertheless, prenatal diagnosis allows for a better postnatal management.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital. Ultrasonography, Prenatal

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  • (PMID = 20074764.001).
  • [ISSN] 1776-257X
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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18. Ababneh K, Al-Khateeb T: Aggressive pregnancy tumor mimicking a malignant neoplasm: a case report. J Contemp Dent Pract; 2009;10(6):E072-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Aggressive pregnancy tumor mimicking a malignant neoplasm: a case report.
  • AIM: The aim of this report is to present the management of an aggressive, highly proliferative pregnancy tumor with clinical and radiographic characteristics highly suggestive of a malignant neoplasm.
  • BACKGROUND: Pregnancy tumor is a benign hyperplastic gingival lesion occurring during pregnancy that is indistinguishable from a pyogenic granuloma arising in nonpregnant females, or in males.
  • CASE DESCRIPTION: A 28-year-old woman at four months of gestation was referred for a massive gingival swelling (5.5 cm in greatest diameter) on the mandibular left side.
  • Advanced alveolar bone loss also was found beneath the lesion.
  • A malignant process was suspected, and an incisional biopsy revealed a pregnancy tumor.
  • SUMMARY: Pregnancy tumor represents an important differential diagnosis of oral masses and can behave in a very aggressive fashion, mimicking a malignant tumor.
  • CLINICAL SIGNIFICANCE: This lesion should always be included in the differential diagnosis of soft tissue masses in a pregnant woman even if the lesion is clinically very aggressive.
  • [MeSH-major] Alveolar Bone Loss / etiology. Gingival Neoplasms / pathology. Gingival Overgrowth / pathology. Granuloma, Pyogenic / pathology. Pregnancy Complications, Neoplastic / pathology
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Mandible. Pregnancy. Treatment Outcome

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  • (PMID = 20020084.001).
  • [ISSN] 1526-3711
  • [Journal-full-title] The journal of contemporary dental practice
  • [ISO-abbreviation] J Contemp Dent Pract
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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19. Vered M, Dobriyan A, Buchner A: Congenital granular cell epulis presents an immunohistochemical profile that distinguishes it from the granular cell tumor of the adult. Virchows Arch; 2009 Mar;454(3):303-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital granular cell epulis presents an immunohistochemical profile that distinguishes it from the granular cell tumor of the adult.
  • Congenital granular cell epulis (CGCE), a rare benign lesion arising from the mucosa of the alveolar ridges of the jaws in newborns, has a clinical course characterized by lack of further growth after birth.
  • Histomorphologically, it resembles a granular cell tumor (GCT) of the adult.
  • This does not confirm any particular cell type for the histogenetic origin of CGCE but may rather reflect a local metabolic or reactive change, providing supporting evidence that the lesion is of a non-neoplastic nature.
  • [MeSH-major] Biomarkers, Tumor / analysis. Gingival Neoplasms / congenital. Gingival Neoplasms / metabolism. Granular Cell Tumor / congenital. Granular Cell Tumor / metabolism

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  • (PMID = 19205730.001).
  • [ISSN] 1432-2307
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Antigens, Differentiation, Myelomonocytic; 0 / Biomarkers, Tumor; 0 / CD68 antigen, human; 0 / S100 Proteins; EC 5.4.2.2 / PGM1 protein, human; EC 5.4.2.2 / Phosphoglucomutase
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20. Pozzi EC, Altermatt HJ, Rees TD, Bornstein MM: Exophytic mass of the gingiva as the first manifestation of metastatic pulmonary adenocarcinoma. J Periodontol; 2008 Jan;79(1):187-91
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Exophytic mass of the gingiva as the first manifestation of metastatic pulmonary adenocarcinoma.
  • BACKGROUND: Metastasis of a malignant tumor to the oral cavity is rare, but it can be the first manifestation of a primary tumor.
  • METHODS: The clinicopathologic features of a gingival metastasis originating from lung adenocarcinoma in a female patient are described.
  • A 57-year-old woman showed a rapidly growing, painless, exophytic mass in the left mandibular gingiva.
  • The intraoral healing after tumor removal was uneventful.
  • CONCLUSIONS: An exophytic lesion on the gingiva can be the first sign of metastatic adenocarcinoma to the oral mucosa.
  • This case emphasizes that even apparently benign-looking gingival lesions in anamnestically healthy patients need to be examined histopathologically.
  • [MeSH-major] Adenocarcinoma / secondary. Gingival Neoplasms / secondary. Lung Neoplasms / diagnosis
  • [MeSH-minor] Biopsy. Diagnosis, Differential. Fatal Outcome. Female. Homeodomain Proteins / analysis. Humans. Immunohistochemistry. Keratin-7 / analysis. Mandible. Middle Aged. Nuclear Proteins / analysis. Transcription Factors / analysis

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  • (PMID = 18166110.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Homeodomain Proteins; 0 / Keratin-7; 0 / Nuclear Proteins; 0 / Transcription Factors; 0 / thyroid nuclear factor 1
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21. Barbuţa OI, Aprodu GS, Gavrilescu S, Mihaila D, Iliev G, Olaru V, Munteanu V, Savu A: [Congenital oropharyngeal tumors in the newborn: problems in team diagnosis and treatment]. Rev Med Chir Soc Med Nat Iasi; 2006 Oct-Dec;110(4):883-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Congenital oropharyngeal tumors in the newborn: problems in team diagnosis and treatment].
  • [Transliterated title] Tumori congenitale cu localizare orofaringiana la nou nascut: probleme de diagnostic şi tratament în echipa.
  • Congenital epulis of the newborn is a rare tumour which is usually benign.
  • Epulis is also known as a congenital gingival granular cell tumour because of its histological features.
  • The histogenesis of the tumour is unknown.
  • Recurrence of the tumour after surgery has not been reported yet.
  • In one case it was an antenatal diagnosis by ultrasonography, in the other it was associated a genital anomalies (hypospadias).
  • [MeSH-major] Gingival Neoplasms / diagnosis. Gingival Neoplasms / surgery. Granular Cell Tumor / diagnosis. Granular Cell Tumor / surgery
  • [MeSH-minor] Diagnosis, Differential. Female. Humans. Infant, Newborn. Male. Treatment Outcome

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  • (PMID = 17438893.001).
  • [ISSN] 0048-7848
  • [Journal-full-title] Revista medico-chirurgicală̆ a Societă̆ţ̜ii de Medici ş̧i Naturaliş̧ti din Iaş̧i
  • [ISO-abbreviation] Rev Med Chir Soc Med Nat Iasi
  • [Language] rum
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Romania
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22. Silva GC, Vieira TC, Vieira JC, Martins CR, Silva EC: Congenital granular cell tumor (congenital epulis): a lesion of multidisciplinary interest. Med Oral Patol Oral Cir Bucal; 2007 Oct;12(6):E428-30

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congenital granular cell tumor (congenital epulis): a lesion of multidisciplinary interest.
  • Congenital granular cell tumor (CGCT), or congenital epulis, is a very uncommon benign soft tissue lesion that usually arises from the alveolar mucosa of neonates and may cause respiratory and feeding problems.
  • We report a case of a 3-day-old female newborn, who presented an intraoral tumor mass which was protruding from her mouth, and compromising feeding.
  • Clinical features and treatment approaches are presented and discussed, emphasizing the necessity of a multidisciplinary approach in such cases.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital

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  • (PMID = 17909507.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Spain
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23. Nouri S, Mahdhaoui N, Bouafsoun C, Zakhama R, Omezzine M, Tahar Yaacoubi M, Salem N, Seboui H: [Obstructive congenital multiple epulis. A case report in a male neonate]. Arch Pediatr; 2008 Jun;15(6):1083-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Congenital epulis or congenital gingival cell tumour is a rare tumour in the neonate.
  • It arises from the gingival mucosa.
  • This benign condition can be life threatening when obstructive.
  • In this report, a case of a male neonate, with features of obstructive congenital epulis arising from both maxillary and mandibular alveolar ridge, interfering with breast-feeding is described.
  • Diagnosis was suspected clinically and confirmed by histology.
  • [MeSH-major] Gingival Neoplasms / pathology. Granular Cell Tumor / pathology

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  • (PMID = 18403186.001).
  • [ISSN] 0929-693X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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24. LeCorn DW, Bhattacharyya I, Vertucci FJ: Peripheral ameloblastoma: a case report and review of the literature. J Endod; 2006 Feb;32(2):152-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Peripheral ameloblastoma is a rare, benign odontogenic tumor that histologically resembles an intraosseous ameloblastoma but develops in the soft tissues of the gingiva and mucosa and exhibits an innocuous clinical behavior.
  • We report a case of a recurrent peripheral ameloblastoma in a 61-year-old man that presented as a painless swelling on the maxillary anterior labial attached gingiva.
  • The peripheral ameloblastoma should be included in the differential diagnosis of a gingival lesion clinically resembling any of the myriads of entities seen on the gingiva including a pyogenic granuloma, peripheral giant cell granuloma, or parulis/gumboil.
  • [MeSH-major] Ameloblastoma / pathology. Gingival Neoplasms / pathology
  • [MeSH-minor] Diagnosis, Differential. Humans. Male. Maxilla. Middle Aged. Neoplasm Recurrence, Local

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  • (PMID = 16427467.001).
  • [ISSN] 0099-2399
  • [Journal-full-title] Journal of endodontics
  • [ISO-abbreviation] J Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 11
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25. Perrotti V, Rubini C, Fioroni M, Iezzi G: Pleomorphic lipoma of the oral cavity. Report of a case. Minerva Stomatol; 2006 May;55(5):321-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pleomorphic lipoma of the oral cavity. Report of a case.
  • Pleomorphic lipoma (PL) is a rare benign tumor mainly located in the upper back, upper shoulders, and back of the neck in elderly men.
  • The differential diagnosis should be made with sclerosing liposarcoma and well-differentiated liposarcoma.
  • A 59-year-old male patient was referred for the presence of a lesion involving the marginal and adherent gingiva of teeth # 5; this lesion extended into the vestibular mucosa.
  • The lesion had a 2 cm diameter, showed no tenderness, had a hard-parenchymatous consistency, was mobile on the underlying tissues and was covered by normal appearing mucosa.
  • A free gingival graft from the palate was used to cover the defect.
  • The definitive pathologic diagnosis was pleomorphic lipoma.
  • Local excision is adequate for PL and the tumor does not recur.
  • [MeSH-major] Gingival Neoplasms / diagnosis. Lipoma / diagnosis
  • [MeSH-minor] Adipocytes / pathology. Diagnosis, Differential. Humans. Liposarcoma / diagnosis. Male. Middle Aged. Stromal Cells / pathology

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  • (PMID = 16688109.001).
  • [ISSN] 0026-4970
  • [Journal-full-title] Minerva stomatologica
  • [ISO-abbreviation] Minerva Stomatol
  • [Language] eng; ita
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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26. Tandon P, Malik R, Tandon R: Congenital epulis of the newborn: a case report with review of literature. Indian J Pathol Microbiol; 2007 Jul;50(3):593-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Congenital epulis, also known as congenital gingival granular cell tumor, is a rare benign intraoral tumor found only in the new born.
  • Antepartum detection by careful imaging and coordination of multidisciplinary team of maternal-fetal medicine, neonatal-perinatal medicine, anesthesiology and otolaryngology and finally the histopathologists who confirm the diagnosis is essential as the histology differentiates it from other congenital intraoral masses like haemangioma, fibroma, rhabdomyoma, rhabdomyosarcoma, lymphangioma, osteogenic and chondrogenic sarcomas.
  • [MeSH-major] Gingival Neoplasms / congenital. Neoplasms, Squamous Cell / congenital

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  • (PMID = 17883149.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] India
  • [Number-of-references] 5
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27. González-Martín-Moro J, Cebrián-Carretero JL, Gómez-García E, del Castillo-Pardo de Vera JL, del Val D: Intraoral tumor with rapid growing. Report of a case. Med Oral Patol Oral Cir Bucal; 2005 Nov-Dec;10(5):440-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intraoral tumor with rapid growing. Report of a case.
  • Most are benign lesions, but some are primary malignancies.
  • [MeSH-major] Abdominal Neoplasms / pathology. Adenocarcinoma / secondary. Gingival Neoplasms / secondary

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  • (PMID = 16264378.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng; spa
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Spain
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28. Scariot R, Giovanini AF, Torres-Pereira CC, Piazzetta CM, Costa DJ, Rebellato NL, Müller PR: Massive growth of an intraoral lipoma. J Contemp Dent Pract; 2008;9(7):115-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Lipoma, a benign tumor of adipose tissue, is rarely seen in the oral cavity.
  • When it does occur it is usually found in the cheek or tongue, followed by the lip, gingival, and floor of the mouth.
  • REPORT: A 71-year-old male with a movable and huge mass located in the buccal mucosa region, which was first noticed approximately 25 years earlier, was referred to the Maxillofacial Surgery Clinic at the Universidade Federal do Paraná.
  • A clinical diagnosis of lipoma was established, and the treatment consisted of complete excision of the mass under local anesthesia.
  • CLINICAL SIGNIFICANCE: This case report emphasizes the slow growth and benign characteristics of oral lipomas.
  • [MeSH-minor] Aged. Humans. Male. Mouth Mucosa / pathology

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  • (PMID = 18997924.001).
  • [ISSN] 1526-3711
  • [Journal-full-title] The journal of contemporary dental practice
  • [ISO-abbreviation] J Contemp Dent Pract
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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29. Braga-Tavares H, Santos H, M-Pinto I, Ramos M, de Sousa P: [Congenital epulis]. Cir Pediatr; 2009 Jan;22(1):49-51

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Congenital epulis or gingival granular cell tumor is an uncommon benign tumor, usually diagnosed at birth as a pediculated maxilar gingival mass.
  • [MeSH-major] Gingival Neoplasms

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  • (PMID = 19323084.001).
  • [ISSN] 0214-1221
  • [Journal-full-title] Cirugía pediátrica : organo oficial de la Sociedad Española de Cirugía Pediátrica
  • [ISO-abbreviation] Cir Pediatr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 28
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30. Park JY, Kim HS, Zo JI, Lee S, Choi SW: Initial presentation of lung sarcomatoid carcinoma as a metastatic lesion in the mandibular gingiva. J Periodontol; 2006 Apr;77(4):734-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Initial presentation of lung sarcomatoid carcinoma as a metastatic lesion in the mandibular gingiva.
  • BACKGROUND: Sarcomatoid carcinoma of the lung is a very rare type of tumor characterized by distant metastasis.
  • However, metastasis to the gingiva is an uncommon event.
  • Occasionally, an oral metastatic lesion may be the preliminary clinical feature observed before the diagnosis of the primary tumor.
  • METHODS: The clinical features of gingival metastasis as an initial presentation of lung sarcomatoid carcinoma are discussed.
  • A 55-year-old male patient presented with a rapidly growing pedunculated exophytic mass on the gingiva at the left side of the lower jaw.
  • RESULTS: The histologic and immunohistochemical diagnosis was metastatic carcinoma.
  • To locate the primary tumor, we analyzed the lung lesion by chest computerized tomography (CT) scans and biopsy.
  • The patient was ultimately diagnosed with sarcomatoid carcinoma of the lung with gingival metastasis.
  • The gingival lesion disappeared after chemotherapy.
  • CONCLUSION: Although this case is unusual, periodontists should recognize that gingival masses similar to benign or inflammatory lesions may represent an initial sign of underlying malignant tumors.
  • [MeSH-major] Carcinoma / secondary. Gingival Neoplasms / secondary. Lung Neoplasms / pathology. Sarcoma / secondary

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  • (PMID = 16584358.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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31. Chi AC, Barnes JD, Budnick S, Agresta SV, Neville B: Rhabdomyosarcoma of the maxillary gingiva. J Periodontol; 2007 Sep;78(9):1839-45
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma of the maxillary gingiva.
  • BACKGROUND: Rhabdomyosarcoma is a malignant neoplasm of primitive mesenchyme exhibiting skeletal muscle differentiation.
  • METHODS: A 33-year-old woman presented with an erythematous gingival mass involving the anterior maxillary gingiva.
  • Many of the tumor cells exhibited abundant eosinophilic cytoplasm.
  • Immunohistochemical stains showed the tumor cells to be positive for desmin, myogenin, and myogenic differentiation 1 (MyoD1).
  • A diagnosis of embryonal rhabdomyosarcoma was made.
  • Pain is a variable presenting symptom, and early lesions may be mistaken for benign neoplastic, inflammatory, or infectious processes.
  • [MeSH-major] Gingival Neoplasms / pathology. Rhabdomyosarcoma / pathology

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  • (PMID = 17760557.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 51
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32. Safadi RA, Hellstein JW, Diab MM, Hammad HM: Nerve sheath myxoma (neurothekeoma) of the gingiva, a case report and review of the literature. Head Neck Pathol; 2010 Sep;4(3):242-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Nerve sheath myxoma (neurothekeoma) of the gingiva, a case report and review of the literature.
  • Nerve sheath myxoma (NSM) is a benign peripheral nerve sheath tumor that rarely occurs in the oral cavity.
  • Among the 23 reported intraoral cases, no lesion has previously been reported on the gingiva.
  • In this report, we describe the first gingival case of oral neurothekeoma with histopathologic and immunohistochemical characteristics.
  • The patient, a 32 year old female presented with a slowly growing gingival mass diagnosed clinically as an epulis.
  • Immunohistochemically, the tumor cells were sporadically positive for S-100 and NSE and negative for GFAP, EMA, SMA, CD68 and HMB45.
  • [MeSH-major] Gingival Neoplasms / pathology. Neurothekeoma / pathology
  • [MeSH-minor] Adult. Biomarkers, Tumor / metabolism. Female. Gingiva. Humans. Schwann Cells / metabolism. Schwann Cells / pathology. Treatment Outcome

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  • [Cites] Int J Oral Maxillofac Surg. 2002 Aug;31(4):451-4 [12361085.001]
  • [Cites] Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2000 Jul;90(1):74-7 [10884639.001]
  • [Cites] Oral Dis. 2001 May;7(3):196-9 [11495197.001]
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  • (PMID = 20502996.001).
  • [ISSN] 1936-0568
  • [Journal-full-title] Head and neck pathology
  • [ISO-abbreviation] Head Neck Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  • [Other-IDs] NLM/ PMC2923317
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33. Laco J: [Congenital granular cell epulis: a case report]. Cesk Patol; 2009 Oct;45(4):117-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Congenital granular cell epulis is a rare benign lesion occuring exclusively in newborns as a solitary or multiple swelling of alveolar mucosa of either maxilla or mandible.
  • A case of a female newborn who presented with multiple swellings of both maxillary and mandibular alveolar mucosa measuring up to 10 mm is presented.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital

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  • (PMID = 20301840.001).
  • [ISSN] 1210-7875
  • [Journal-full-title] Československá patologie
  • [ISO-abbreviation] Cesk Patol
  • [Language] cze
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Czech Republic
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34. Ruschel HC, Beilke LP, Beilke RP, Kramer PF: Congential epulis of newborn: report of a spontaneous regression case. J Clin Pediatr Dent; 2008;33(2):167-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Congential epulis of newborn: report of a spontaneous regression case.
  • Congenital epulis of newborn is a rare benign tumor that is also known as a congenital granular cell tumor.
  • The objective of this article was to describe and discuss the case of a newborn girl with a pedunculated mass in the left anterior maxillary alveolar margin diagnosed as congenital epulis.
  • [MeSH-major] Alveolar Process / surgery. Gingival Neoplasms / surgery. Maxillary Neoplasms / surgery
  • [MeSH-minor] Female. Humans. Infant, Newborn. Mouth Mucosa / pathology. Mouth Mucosa / surgery. Treatment Outcome

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  • (PMID = 19358386.001).
  • [ISSN] 1053-4628
  • [Journal-full-title] The Journal of clinical pediatric dentistry
  • [ISO-abbreviation] J Clin Pediatr Dent
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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35. Ben Hamouda H, Ayat A, Elloumi I, Belaid L, Bouzaiène M, Korbi S, Soua H, Sfar MT: Obstructive congenital epulis. Eur Ann Otorhinolaryngol Head Neck Dis; 2010 May;127(2):86-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • INTRODUCTION: Congenital epulis, known as a congenital gingival granular cell tumor, is a benign tumor and very rare in newborns.
  • DISCUSSION: We report the clinical case of a female full-term newborn who presented a tumor on the upper gum obtruding into the oral cavity discovered at birth.
  • Histological examination confirmed the diagnosis of gingival tumor with granular cells and absence of signs of malignancy.
  • CONCLUSION: Prenatal diagnosis is fundamental in the therapeutic approach to this rare lesion but remains difficult because the findings are non specific and the generally late development of the tumor.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital

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  • [Copyright] Copyright © 2010 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20822763.001).
  • [ISSN] 1879-730X
  • [Journal-full-title] European annals of otorhinolaryngology, head and neck diseases
  • [ISO-abbreviation] Eur Ann Otorhinolaryngol Head Neck Dis
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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36. Wiel J, Luis W, Kempf HG: [The interesting case -- case no. 70]. Laryngorhinootologie; 2005 Mar;84(3):196-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We will report two cases of newborn girls, who could not be breast fed because of a benign tumour in their oral cavity.
  • Tumours were fleshy, firm, dark-brown with a broad-based attachment to the alveolar ridge.
  • The size of neoplasm was in one case 3 x 2 cm, in the other one 2 x 1.5 cm.
  • Histological findings showed large tumour cells with abundant granular eosinophilic cytoplasm and a prominent vascularity.
  • All these findings are characteristic of congenital granular cell tumour and its synonym congenital epulis.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital. Mouth Neoplasms / congenital
  • [MeSH-minor] Age Factors. Breast Feeding. Female. Gingiva / pathology. Humans. Immunohistochemistry. Infant, Newborn. Mouth / pathology. Sex Factors. Treatment Outcome

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  • (PMID = 15770569.001).
  • [ISSN] 0935-8943
  • [Journal-full-title] Laryngo- rhino- otologie
  • [ISO-abbreviation] Laryngorhinootologie
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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37. Levi PA Jr, Kim DM, Harsfield SL, Jacobson ER: Squamous cell carcinoma presenting as an endodontic-periodontic lesion. J Periodontol; 2005 Oct;76(10):1798-804
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Regardless of advances in diagnosis and treatment during the past 40 years, the overall 5-year survival rates for oral and oropharyngeal squamous cancers have only slightly improved and remain around 50%.
  • Thus, the early diagnosis and treatment of carcinoma by health care providers are essential in achieving a good prognosis.
  • We report a case of invasive squamous cell carcinoma that presented as a benign endodontic-periodontic lesion with a 7-mm periodontal pocket on tooth #15 in a 40-year-old, non-smoking woman.
  • The patient remained free of tumor for 5 years after the initial presentation.
  • [MeSH-major] Carcinoma, Squamous Cell / pathology. Gingival Neoplasms / pathology. Maxillary Neoplasms / pathology. Periodontal Cyst / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Maxillary Sinus Neoplasms / pathology. Neoplasm Invasiveness / pathology

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  • (PMID = 16253104.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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38. Prado JD, Andrade RG, Silva-Sousa YT, Andrade MF, Soares FA, Perez DE: Nerve sheath myxoma of the gingiva: report of a rare case and review of the literature. J Periodontol; 2007 Aug;78(8):1639-43

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Nerve sheath myxoma of the gingiva: report of a rare case and review of the literature.
  • BACKGROUND: Nerve sheath myxoma (NSM) is an extremely rare benign neoplasm in the oral cavity.
  • This paper describes the first case, to our knowledge, of NSM in the gingival mucosa of an 84-year-old female patient.
  • METHODS: Intraoral examination revealed a painless and well-defined nodule in the lingual gingival mucosa of the right mandibular lateral incisor, which measured approximately 1.0 cm in diameter.
  • A trauma-induced gingival hyperplasia was the main diagnostic hypothesis.
  • According to the histopathologic and immunohistochemical features, the diagnosis of NSM was established.
  • CONCLUSION: Although NSM is an extremely rare oral tumor, it should be considered in the clinical differential diagnosis of gingival nodules.
  • [MeSH-major] Gingival Neoplasms / diagnosis. Myxoma / diagnosis. Nerve Sheath Neoplasms / diagnosis
  • [MeSH-minor] Aged, 80 and over. Diagnosis, Differential. Female. Follow-Up Studies. Gingival Hyperplasia / diagnosis. Humans. Incisor / pathology. Mandible / pathology. S100 Proteins / analysis. Vimentin / analysis

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  • (PMID = 17668985.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / S100 Proteins; 0 / Vimentin
  • [Number-of-references] 28
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39. Rinaggio J, Cleveland D, Koshy R, Gallante A, Mirani N: Peripheral granular cell odontogenic fibroma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 Nov;104(5):676-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Peripheral odontogenic fibroma is a rare lesion that arises on the gingiva and can clinically mimic a variety of reactive lesions, benign neoplasms, and metastases.
  • We describe a symptomatic lesion arising on the mandibular gingiva of a 58-year-old female with no history of trauma or dental disease in the area.
  • [MeSH-major] Fibroma / pathology. Gingival Neoplasms / pathology. Granular Cell Tumor / pathology. Mandibular Neoplasms / pathology. Odontogenic Tumors / pathology

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  • (PMID = 17223586.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 68238-35-7 / Keratins
  • [Number-of-references] 8
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40. Colombo P, Tondulli L, Masci G, Muzza A, Rimassa L, Petrella D, Santoro A: Oral ulcer as an exclusive sign of gastric cancer: report of a rare case. BMC Cancer; 2005;5:117
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Oral ulcer as an exclusive sign of gastric cancer: report of a rare case.
  • BACKGROUND: The oral cavity is a rare but occasional target for metastases, which may masquerade as various benign and inflammatory lesions, and sometimes also be asymptomatic.
  • CASE PRESENTATION: We here describe an uncommon case of a hard palate mucosa and gingival metastasis from gastric carcinoma that was originally diagnosed as a periodontal disease.
  • Histopathological examination of a biopsy of the lesion revealed a signet-ring cell carcinoma, and a subsequent biopsy of an ulcerated stomach lesion showed a poorly differentiated gastric carcinoma.
  • The patient underwent gastric resection but died of heart failure on the tenth postoperative day; a post-mortem examination revealed a residual bilateral ovarian infiltration by gastric carcinoma (Krukenberg's tumor).
  • CONCLUSION: An occult carcinoma of the stomach may rarely metastasise to the oral cavity even as a first and exclusive manifestation; it is important to bear this possibility in mind because such conditions may mimic a benign disease.
  • [MeSH-major] Carcinoma, Signet Ring Cell / diagnosis. Carcinoma, Signet Ring Cell / pathology. Gingival Neoplasms / secondary. Mouth / pathology. Mouth Neoplasms / secondary. Stomach Neoplasms / diagnosis. Stomach Neoplasms / pathology. Ulcer / pathology
  • [MeSH-minor] Biopsy. Carcinoma / pathology. Cell Differentiation. Fatal Outcome. Female. Humans. Immunohistochemistry. Middle Aged. Mouth Mucosa / pathology. Neoplasm Metastasis. Palate, Hard / pathology

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  • [Cites] J Periodontol. 1976 Jun;47(6):358-60 [1064724.001]
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  • (PMID = 16171522.001).
  • [ISSN] 1471-2407
  • [Journal-full-title] BMC cancer
  • [ISO-abbreviation] BMC Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1242220
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41. Azevedo Rde S, Pires FR, Della Coletta R, de Almeida OP, Kowalski LP, Lopes MA: Oral myofibromas: report of two cases and review of clinical and histopathologic differential diagnosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Jun;105(6):e35-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Oral myofibromas: report of two cases and review of clinical and histopathologic differential diagnosis.
  • Myofibroma is a benign mesenchymal neoplasm composed of myofibroblasts which has been described with different synonyms since the first report in 1951.
  • Differential diagnosis included benign and malignant mesenchymal neoplasms, salivary gland tumors, and reactive processes.
  • Microscopic analysis of both lesions revealed a spindle cell tumor with immunoreactivity for vimentin, muscle-specific actin, and specific smooth muscle isoform alpha-actin, rendering the diagnoses of myofibroma.
  • Myofibroma presents a wide range of differential diagnosis, including benign and malignant neoplasms.
  • Therefore, accurate diagnosis may avoid an unnecessary aggressive therapy.
  • [MeSH-major] Gingival Neoplasms / pathology. Lip Neoplasms / pathology. Myofibroma / pathology
  • [MeSH-minor] Actins / analysis. Child. Diagnosis, Differential. Humans. Immunohistochemistry. Male. Vimentin / analysis

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  • (PMID = 18417385.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Actins; 0 / Vimentin
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42. Olson JL, Marcus JR, Zuker RM: Congenital epulis. J Craniofac Surg; 2005 Jan;16(1):161-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Congenital epulis is a rare benign hamartoma of the alveolar ridge found in the newborn.
  • The diagnosis, pathology, and treatment are reviewed.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital
  • [MeSH-minor] Diagnosis, Differential. Female. Gingival Diseases / congenital. Hamartoma / congenital. Humans. Infant, Newborn. Maxilla

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  • (PMID = 15699667.001).
  • [ISSN] 1049-2275
  • [Journal-full-title] The Journal of craniofacial surgery
  • [ISO-abbreviation] J Craniofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 16
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43. López-Jornet P, Bermejo-Fenoll A: Peripheral ameloblastoma of the gingiva: the importance of diagnosis. J Clin Periodontol; 2005 Jan;32(1):12-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Peripheral ameloblastoma of the gingiva: the importance of diagnosis.
  • BACKGROUND: Peripheral ameloblastoma is an extremely rare epithelial odontogenic tumor, limited to the soft tissues of the gums or oral mucosa.
  • Although the lesion is benign, it may be locally aggressive.
  • METHODS: The present study describes the case of a 31-year-old male presenting a firm, symptomless tumor mass of irregular appearance and measuring approximately 12 mm in diameter, located in the distal zone of 4.7.
  • The cells in the peripheral zone adopted a palisade distribution, and presented the appearance of a lax reticulum at central level.
  • The diagnosis was peripheral ameloblastoma.
  • [MeSH-major] Ameloblastoma / pathology. Gingival Diseases / pathology

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  • [Copyright] Copyright Blackwell Munksgaard, 2004.
  • (PMID = 15642052.001).
  • [ISSN] 0303-6979
  • [Journal-full-title] Journal of clinical periodontology
  • [ISO-abbreviation] J. Clin. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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44. Yalçin F, Yalçin S, Berber L, Gür H: Peripheral giant cell granuloma combined with facial hemangioma. A case report. J Int Acad Periodontol; 2005 Oct;7(4):108-13
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Peripheral giant cell granuloma (PGCG) is a relatively uncommon benign tumor of the oral cavity affecting people of all ages and with no racial predilection.
  • Hemangioma is a benign process in which there are an increased number of normal or abnormal-appearing blood vessels.
  • In this article the clinical, radiographic and histopathologic characteristics of a patient who had a rare combination of PGCG and facial hemangioma is discussed.
  • [MeSH-major] Facial Neoplasms / complications. Gingival Diseases / complications. Granuloma, Giant Cell / complications. Hemangioma / complications. Skin Neoplasms / complications

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  • (PMID = 16245641.001).
  • [ISSN] 1466-2094
  • [Journal-full-title] Journal of the International Academy of Periodontology
  • [ISO-abbreviation] J Int Acad Periodontol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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45. Williams RW, Grave B, Stewart M, Heggie AA: Prenatal and postnatal management of congenital granular cell tumours: a case report. Br J Oral Maxillofac Surg; 2009 Jan;47(1):56-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Congenital granular cell tumour is a rare, benign, soft tissue lesion of the oral cavity.
  • Large or multiple lesions can cause mechanical obstruction of the oral cavity and may result in prenatal polyhydramnios, and postnatal feeding and respiratory problems.We present a case in which prenatal diagnostic imaging was used in the successful management of an infant with a large congenital granular cell tumour.
  • [MeSH-major] Gingival Neoplasms / diagnosis. Gingival Neoplasms / surgery. Granular Cell Tumor / congenital. Granular Cell Tumor / diagnosis. Ultrasonography, Prenatal

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  • (PMID = 18556098.001).
  • [ISSN] 1532-1940
  • [Journal-full-title] The British journal of oral & maxillofacial surgery
  • [ISO-abbreviation] Br J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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46. Chtourou I, Krichen Makni S, Dhouib M, Khabir A, Fakhfakh I, Ayadi L, Mnif H, Abdelmoula M, Sellami Boudawara T: [Pediatric mandibular myofibromatosis]. Rev Stomatol Chir Maxillofac; 2007 Nov;108(5):461-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Myofibromatose infantile de la mandibule.
  • INTRODUCTION: Pediatric myofibromatosis is a rare tumor in neonates and children.
  • The aim of this article was to report the anatomoclinical and therapeutic features of this pediatric tumor in a case as well as its follow-up.
  • CASE REPORT: A 10-year-old girl was brought to consultation for a lower left gingival swelling 5 cm in diameter, forming a unit with the mandibular bone.
  • Imagery revealed the presence of an osteolytic tumor benign in aspect, but locally aggressive.
  • The diagnosis of pediatric myofibromatosis was confirmed.
  • The diagnosis is made on anatomopathological findings and immunohistochemical assessment.

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  • (PMID = 17632191.001).
  • [ISSN] 0035-1768
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Actins; 0 / Vimentin
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47. Koyuncu BO, Zeytinoğlu M, Unal T, Zeytinoğlu B: Myofibroma of the gingiva: report of a case. J Clin Pediatr Dent; 2010;34(3):253-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Myofibroma of the gingiva: report of a case.
  • Myofibroma is a benign mesenchymal neoplasm composed of myofibroblasts which has been described with different synonyms since the first report in 1951.
  • Awareness and recognition of this benign tumor is important to establish the correct diagnosis and avoid morbidity of unnecessary aggressive therapy.
  • This report describes a myofibroma of the gingiva in a 14 year old girl and is reported together with the conventional histologic, and immunohistochemical findings.
  • The tumor showed rapid increase in size and clinical features suggestive of malignancy.
  • However on histopathologic evaluation it was diagnosed as a benign neoplasm, and this diagnosis was supported by immunohistochemical markers.
  • [MeSH-major] Gingival Neoplasms / diagnosis. Myofibroma / diagnosis
  • [MeSH-minor] Actins / analysis. Adolescent. Desmin / analysis. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Immunohistochemistry. S100 Proteins / analysis. Vimentin / analysis

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  • (PMID = 20578664.001).
  • [ISSN] 1053-4628
  • [Journal-full-title] The Journal of clinical pediatric dentistry
  • [ISO-abbreviation] J Clin Pediatr Dent
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Actins; 0 / Desmin; 0 / S100 Proteins; 0 / Vimentin
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48. Rashmi MS, Alka KD, Seema C: Oral hobnail hemangioma--a case report. Quintessence Int; 2008 Jun;39(6):507-10
MedlinePlus Health Information. consumer health - Birthmarks.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Hobnail hemangioma is a rare benign vascular tumor.
  • The present article reports a case of hobnail hemangioma on the mandibular left gingiva in a 24-year-old male patient.
  • Awareness of this rare entity rests on the differential diagnosis, which includes retiform hemangioendothelioma, patch-stage Kaposi sarcoma, benign lymphangioendothelioma, and well-differentiated angiosarcoma.
  • [MeSH-major] Gingival Neoplasms / pathology. Hemangioma / pathology
  • [MeSH-minor] Diagnosis, Differential. Endothelial Cells / pathology. Humans. Male. Young Adult

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  • (PMID = 19057748.001).
  • [ISSN] 1936-7163
  • [Journal-full-title] Quintessence international (Berlin, Germany : 1985)
  • [ISO-abbreviation] Quintessence Int
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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49. Oda D: Soft-tissue lesions in children. Oral Maxillofac Surg Clin North Am; 2005 Nov;17(4):383-402

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • This article reviews some of the benign and malignant oral soft-tissue swellings that occur in children, with an emphasis on their clinical presentation, etiology, histopathology, and treatment.
  • These lesions include single and multiple nodules, reactive lesions, and benign and malignant neoplasms.
  • Diseases discussed include reactive gingival swelling, generalized gingival fibromatosis, melanotic neuroectodermal tumor of infancy, fibromas, vascular lesions, salivary gland lesions, and infantile rhabdomyomas.
  • Also covered are lesions that may present in multiples, such as neuromas, multiple endocrine neoplasia type 2b, neurofibromatosis, and human papilloma virus-related benign epithelial lesions.
  • Benign but locally aggressive and malignant neoplasms are discussed, such as aggressive fibromatosis, myofibromatosis, fibrosarcoma, and rhabdomyosarcoma.

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  • (PMID = 18088794.001).
  • [ISSN] 1042-3699
  • [Journal-full-title] Oral and maxillofacial surgery clinics of North America
  • [ISO-abbreviation] Oral Maxillofac Surg Clin North Am
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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50. Kim K, Velez I, Kaltman SI, Lopez E, Stern D: Odontogenic carcinoma differentiation into rhabdomyosarcoma: report of a rare case. Quintessence Int; 2009 Nov-Dec;40(10):837-42

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Odontogenic carcinoma differentiation into rhabdomyosarcoma: report of a rare case.
  • The histology and clinical features of this aggressive odontogenic neoplasm are described.
  • Within the English-language literature, only 2 cases are reported of an odontogenic tumor with muscle differentiation: a benign odontogenic tumor (ameloblastoma) with differentiation into a rhabdomyosarcoma and an odontogenic sarcoma with smooth-muscle differentiation.
  • [MeSH-major] Gingival Neoplasms / pathology. Neoplasms, Multiple Primary / pathology. Odontogenic Tumors / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Aged. Biopsy. Diagnosis, Differential. Follow-Up Studies. Gingival Diseases / diagnosis. Granuloma, Giant Cell / diagnosis. Granuloma, Pyogenic / diagnosis. Humans. Male. Maxillary Neoplasms / pathology

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  • (PMID = 19898715.001).
  • [ISSN] 1936-7163
  • [Journal-full-title] Quintessence international (Berlin, Germany : 1985)
  • [ISO-abbreviation] Quintessence Int
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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51. Kumar Dutta H: Jaw and gum tumours in children. Pediatr Surg Int; 2009 Sep;25(9):781-4
MedlinePlus Health Information. consumer health - Jaw Injuries and Disorders.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Jaw and gum tumours in children.
  • INTRODUCTION: Jaw and gum tumours are rare conditions in children.
  • MATERIALS AND METHODS: Fourteen children presenting with jaw and gum tumours are retrospectively analysed.
  • Melanotic neuroectodermal tumour of infancy was noted in two patients.
  • Ameloblastic fibrosis, another rare tumour in children, and non-osseus fibroma were noted in one patient each.
  • CONCLUSION: Jaw and gum tumours in children are usually benign.
  • Excision of the tumour or curettage is curative in most of them.
  • [MeSH-major] Gingival Diseases / pathology. Jaw Diseases / pathology
  • [MeSH-minor] Bone Cysts, Aneurysmal / pathology. Bone Cysts, Aneurysmal / surgery. Child. Child, Preschool. Curettage. Edema / etiology. Female. Fibroma / pathology. Fibroma / surgery. Follow-Up Studies. Granuloma, Giant Cell / pathology. Granuloma, Giant Cell / surgery. Humans. Infant. Infant, Newborn. Male. Neuroectodermal Tumor, Melanotic / pathology. Neuroectodermal Tumor, Melanotic / surgery. Pain / etiology. Retrospective Studies

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  • [Cites] Arch Dis Child. 1989 Jan;64(1):145-7 [2923466.001]
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  • (PMID = 19669649.001).
  • [ISSN] 1437-9813
  • [Journal-full-title] Pediatric surgery international
  • [ISO-abbreviation] Pediatr. Surg. Int.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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52. Mabongo M, Wood NH, Lemmer J, Feller L: Congenital epulis. A case report. SADJ; 2008 Jul;63(6):350-1

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • It is a benign hamartoma that may interfere with feeding and respiration.
  • [MeSH-major] Gingival Neoplasms / congenital. Granular Cell Tumor / congenital

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  • (PMID = 18811099.001).
  • [ISSN] 1029-4864
  • [Journal-full-title] SADJ : journal of the South African Dental Association = tydskrif van die Suid-Afrikaanse Tandheelkundige Vereniging
  • [ISO-abbreviation] SADJ
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] South Africa
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53. Abo-Hager EA, Khater DS, Ahmed MM: Exploration of the histogenesis of congenital granular cell epulis: an immunohistochemical study. J Egypt Natl Canc Inst; 2009 Jun;21(2):77-83

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • OBJECTIVE: Congenital granular cell epulis is a benign soft tissue lesion of the neonate that arises from the alveolar ridges of the jaws in newborns.
  • [MeSH-major] Biomarkers, Tumor / analysis. Gingival Neoplasms / metabolism. Gingival Neoplasms / pathology. Granular Cell Tumor / metabolism. Granular Cell Tumor / pathology

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  • (PMID = 21057558.001).
  • [ISSN] 1110-0362
  • [Journal-full-title] Journal of the Egyptian National Cancer Institute
  • [ISO-abbreviation] J Egypt Natl Canc Inst
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Egypt
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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54. Rader C, Piorkowski J, Bass DM, Babigian A: Epulis gravidarum manum: pyogenic granuloma of the hand occurring in pregnant women. J Hand Surg Am; 2008 Feb;33(2):263-5
MedlinePlus Health Information. consumer health - Skin Conditions.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Pyogenic granuloma, also known as lobular capillary hemangioma, is a benign vascular tumor of the skin and mucous membranes.
  • Whereas the literature describes pyogenic granulomas of pregnancy as occurring mainly within the gingival or oral mucosa, we present 5 cases of a histologically confirmed pyogenic granuloma on the hands of gravid women, each with no history of antecedent trauma.

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  • MedlinePlus Health Information. consumer health - Health Problems in Pregnancy.
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  • (PMID = 18294552.001).
  • [ISSN] 0363-5023
  • [Journal-full-title] The Journal of hand surgery
  • [ISO-abbreviation] J Hand Surg Am
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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