Case Reports in Otolaryngology最新文献_第6页

Alobar Holoprosencephaly with Cebocephaly in a Neonate Born to an HIV-Positive Mother in Eastern Uganda. 乌干达东部一名艾滋病毒阳性母亲所生的新生儿无前脑畸形伴头畸形。

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Case Reports in Otolaryngology Pub Date : 2021-10-25 eCollection Date: 2021-01-01 DOI: 10.1155/2021/7282283

Franck Katembo Sikakulya, Sonye Magugu Kiyaka, Robert Masereka, Robinson Ssebuufu

引用次数: 3

Deep Neck Infection: Atypical Presentation of Papillary Thyroid Cancer. 深颈部感染:甲状腺乳头状癌的不典型表现。

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Case Reports in Otolaryngology Pub Date : 2021-10-18 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1479201

Apichana Mahattanapreut, Rangsima Aroonroch, Chalermchai Chintrakarn, Chutintorn Sriphrapradang

{"title":"Deep Neck Infection: Atypical Presentation of Papillary Thyroid Cancer.","authors":"Apichana Mahattanapreut, Rangsima Aroonroch, Chalermchai Chintrakarn, Chutintorn Sriphrapradang","doi":"10.1155/2021/1479201","DOIUrl":"https://doi.org/10.1155/2021/1479201","url":null,"abstract":"Deep neck infection is defined as an infectious process in the potential spaces and fascial plane of the neck which may result in a fatal complication. Prompt drainage and broad-spectrum antibiotics are the mainstays of treatment. Deep neck infection as the initial presentation of primary head and neck cancer is not common. Nevertheless, head and neck squamous cell carcinoma is the most common primary head and neck cancer, which could present with cervical metastasis and subsequently becomes infected. Papillary thyroid cancer has a naturally indolent course, and most patients present with a thyroid nodule. However, deep neck infection could be an uncommon presentation of papillary thyroid cancer which may obscure the diagnosis of underlying malignancy. This case report aims to present a rare presentation of papillary thyroid cancer which needs meticulous evaluation. Moreover, the pathological examination should be performed in all cases of deep neck infection for early detection and management of underlying papillary thyroid cancer.","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"1479201"},"PeriodicalIF":0.6,"publicationDate":"2021-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553508/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39832666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

A Case of Nasopharyngeal Mycobacteriosis with Bony Erosion of the External Skull Base. 鼻咽分枝杆菌病合并外颅底骨侵蚀1例。

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Case Reports in Otolaryngology Pub Date : 2021-10-15 eCollection Date: 2021-01-01 DOI: 10.1155/2021/7500273

Kohei Matsuo, Satoshi Tanaka, Masayuki Sakata, Hiroki Takeda, Akihiro Nagata, Masashi Mori, Rie Ito, Yoshifumi Yamamoto, Kiyonobu Ueno, Atsuhiko Uno

{"title":"A Case of Nasopharyngeal Mycobacteriosis with Bony Erosion of the External Skull Base.","authors":"Kohei Matsuo, Satoshi Tanaka, Masayuki Sakata, Hiroki Takeda, Akihiro Nagata, Masashi Mori, Rie Ito, Yoshifumi Yamamoto, Kiyonobu Ueno, Atsuhiko Uno","doi":"10.1155/2021/7500273","DOIUrl":"https://doi.org/10.1155/2021/7500273","url":null,"abstract":"Primary nasopharyngeal mycobacteriosis is a rare disease. We present a case in which skull base bone erosion appeared and was alleviated during the course of the treatment. Bone complications occur in osteoarticular mycobacteriosis, but their occurrence in primary nasopharyngeal mycobacteriosis has not been reported. A 77-year-old immunocompromised Asian woman presented with a right occipitotemporal headache. An ulcerative mass covered with a thick yellowish discharge was found in the roof and posterior walls of the right nasopharynx. Because histopathological examination indicated the presence of mycobacterial infection, we began using antituberculosis medication for the treatment because of the possibility of primary nasopharyngeal tuberculosis. However, this was followed by glossopharyngeal and vagus nerve paralysis. Computed tomography (CT) showed a diffuse enhancing mucosal irregularity in the nasopharynx with bony erosion of the external skull base. Deep tissue biopsy was repeated to differentiate it from malignant lesions, and drainage of pus from the right nasopharynx was confirmed. Subsequently, the headache, neurological findings, and the yellowish discharge disappeared, and the bony erosion of the external skull base was alleviated. Surgical intervention should also be considered for drug-resistant mycobacteriosis. We concluded that mycobacteriosis should also be considered apart from carcinoma even if CT shows a diffuse enhancing mucosal irregularity with bone destruction in the nasopharynx.","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"7500273"},"PeriodicalIF":0.6,"publicationDate":"2021-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536460/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39555441","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Arteriovenous Malformation in the Auricle in a 59-Year-Old Woman. 59岁女性耳廓动静脉畸形1例。

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Case Reports in Otolaryngology Pub Date : 2021-10-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/7438571

Junhui Jeong

引用次数: 1

Survival of Toddler with Aortoesophageal Fistula after Button Battery Ingestion. 儿童误食纽扣电池后主动脉食管瘘的存活率。

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Case Reports in Otolaryngology Pub Date : 2021-10-05 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5557054

Hannah Gibbs, Rishabh Sethia, Patrick I McConnell, Jennifer H Aldrink, Toshiharu Shinoka, Kent Williams, Kris R Jatana

引用次数: 5

A Case of Amelanotic Malignant Melanoma of the Lingual Base That Was Diagnosed Based on a Biopsy of Late Metastasis to a Lumbar Vertebra after Being Misdiagnosed as HPV-Positive Oropharyngeal Anterior Wall Squamous Cell Carcinoma. 1例口咽前壁鳞状细胞癌误诊为HPV阳性，经腰椎晚期转移活检诊断为舌根无毛恶性黑色素瘤。

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Case Reports in Otolaryngology Pub Date : 2021-09-30 eCollection Date: 2021-01-01 DOI: 10.1155/2021/7139280

Takumi Okuda, Shinsuke Ide, Kei Kajihara, Tetsuya Tono

{"title":"A Case of Amelanotic Malignant Melanoma of the Lingual Base That Was Diagnosed Based on a Biopsy of Late Metastasis to a Lumbar Vertebra after Being Misdiagnosed as HPV-Positive Oropharyngeal Anterior Wall Squamous Cell Carcinoma.","authors":"Takumi Okuda, Shinsuke Ide, Kei Kajihara, Tetsuya Tono","doi":"10.1155/2021/7139280","DOIUrl":"https://doi.org/10.1155/2021/7139280","url":null,"abstract":"We report a case of amelanotic malignant melanoma (AMM) in a 66-year-old female. AMM of the lingual base was diagnosed based on a biopsy of late metastasis to the bone marrow of the L4 lumbar vertebra. The patient was initially treated with chemoradiotherapy after being misdiagnosed with poorly differentiated human papillomavirus- (HPV-) related squamous cell carcinoma of the oropharyngeal anterior wall. p16 immunostaining is used to diagnose HPV-related oropharyngeal cancer. However, while p16 expression is used as a surrogate marker of HPV infection, it is important to be aware that p16 protein overexpression can also be caused by other factors. Malignant melanoma is known to express the p16 protein. Morphologically differentiating between AMM and poorly differentiated squamous cell carcinoma based on hematoxylin-eosin staining is difficult. Therefore, in cases that are pathologically diagnosed as p16-positive poorly differentiated oropharyngeal squamous cell carcinoma, it is important to rule out AMM.","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"7139280"},"PeriodicalIF":0.6,"publicationDate":"2021-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497148/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39505851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Presence of Two Separate Hairy Polyps with Meningothelial Elements in a 15-Month-Old Child. 一个15个月大的婴儿出现两个独立的毛状息肉并伴有脑膜上皮成分。

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Case Reports in Otolaryngology Pub Date : 2021-09-21 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1844244

Ahmad Saeed A Alghamdi, Nasser Almutairi, Ghassan Alokby

{"title":"Presence of Two Separate Hairy Polyps with Meningothelial Elements in a 15-Month-Old Child.","authors":"Ahmad Saeed A Alghamdi, Nasser Almutairi, Ghassan Alokby","doi":"10.1155/2021/1844244","DOIUrl":"https://doi.org/10.1155/2021/1844244","url":null,"abstract":"Hairy polyps are benign embryological tumors of the head and neck region that are derived from two germinal layers, the ectoderm and mesoderm. At an incidence of 1 : 40000, hairy polyps are considered rare growths. Presenting symptoms of hairy polyps can vary greatly depending on the size and location of the tumor. To the best of our knowledge, our reported case is the first in the literature to highlight an extremely rare occurrence of two separate hairy polyps being simultaneously present in one patient, in the clivus and the nasion, with the presence of meningothelial cells within both tumors, histopathologically. With surgical resection as the management of choice, the approach of surgery differs greatly depending on many factors. Since the patient in our reported case had a cleft palate, we used a combined transnasal and transoral approach to fully release the clival mass and a direct skin incision for the nasion mass. Recurrence after complete surgical resection is rare, and if happens, it should rise suspicion of histopathologically misdiagnosed tumor. We amplified the importance of advanced radiological investigations along with proper multidisciplinary teamwork to exclude CNS connections and other histologically malignant tumors and to early pick up a possible simultaneous lesion.","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"1844244"},"PeriodicalIF":0.6,"publicationDate":"2021-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478528/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39474887","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Nasopharyngeal Coil Dislocation of an Embolized Internal Carotid Artery Pseudoaneurysm. 栓塞性颈内动脉假性动脉瘤鼻咽线圈脱位。

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Case Reports in Otolaryngology Pub Date : 2021-09-11 eCollection Date: 2021-01-01 DOI: 10.1155/2021/4270441

Nazli Ay, Ingo Todt, Holger Sudhoff

{"title":"Nasopharyngeal Coil Dislocation of an Embolized Internal Carotid Artery Pseudoaneurysm.","authors":"Nazli Ay, Ingo Todt, Holger Sudhoff","doi":"10.1155/2021/4270441","DOIUrl":"https://doi.org/10.1155/2021/4270441","url":null,"abstract":"Objective: Severe epistaxis caused by ruptured intracranial pseudoaneurysms can be effectively treated by coil embolization. This is generally an efficient and safe procedure and provides sufficient protection recurrent epistaxis. However, complications such as aneurysm rupture, arterial dissection, bleeding, and emboli can occur. A dislocation of a nasopharyngeal coil is an extremely rare event. Patient. We present a case of a 61-year-old patient with a recurrent undifferentiated nasopharyngeal carcinoma (NPC) treated with severe epistaxis. Initially, epistaxis was successfully controlled by a nasal packing. Recurrent bleeding despite packing required a neuroradiological intervention. An intracranially ruptured pseudoaneurysm was detected by magnetic resonance imaging (MRI) and computed tomography (CT), originating from the internal carotid artery at the junction of the petrous part to the cavernous part. Coiling and endovascular plug embolization was performed for the treatment of aneurysm. Ten months later, the patient removed a foreign body out of his left nose. It was dislocated coil material due to radionecrosis. MRI confirmed sufficient embolization of the internal carotid artery.Conclusions: This case report highlights the possibility of a nasopharyngeal coil dislocation of an embolized internal carotid artery aneurysm emerging as a nasal foreign body.","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"4270441"},"PeriodicalIF":0.6,"publicationDate":"2021-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452431/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39439692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 2

A Rare Case of Posttraumatic Bilateral BPPV Presentation. 一例罕见的创伤后双侧BPPV表现。

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Case Reports in Otolaryngology Pub Date : 2021-09-06 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8636676

Sinisa Maslovara, Andro Kosec, Ivana Pajic Matic, Anamarija Sestak

引用次数: 1

The Rare Cases of Parotid Gland Arteriovenous Malformations. 腮腺动静脉畸形的罕见病例分析。

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Case Reports in Otolaryngology Pub Date : 2021-09-02 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6072155

Manish Gupta, Vijay Shrawan Nijhawan, Cynthia Kaur, Sukhpreet Kaur, Akanksha Gupta

引用次数: 2