scholarly journals Multiple Adult Xanthogranuloma: A Rare Case Report with Characteristics

2021 ◽  
Vol 4 (2) ◽  
pp. 88-92
Author(s):  
Xin Tian ◽  
Suling He ◽  
Runxiang Li ◽  
Jianqin Wang
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Clinical Manifestation ◽  
Rare Case ◽  
Hematological Malignancies ◽  
Clinical Manifestations ◽  
Pathological Features ◽  
Adult Form ◽  
Rare Case Report ◽  
Cutaneous Damage

Multiple adult xanthogranuloma (MAXG) is an uncommon adult form of xanthogranuloma. The clinical manifestation of MAXG is relatively rare, but it has characteristic histopathological and immunohistochemical features. MAXG is mainly associated with cutaneous damage, and extracutaneous manifestations such as cervical spine, intracardiac, and periocular lesions have rarely been reported. In patients with systemic association, clinicians should pay attention to the possibility of hematological malignancies. We report the case of a 17-year-old man with multiple lesions on the head, face, neck, arms and trunk, along with the clinical manifestations and pathological features.

Aneurysmal Bone Cyst of C2, C3 Cervical Spine: A Rare Case Report and Review of Literature

2015 ◽  
Vol 2 (2) ◽  
pp. 52-54
Author(s):  
Vikas Naik ◽  
GC Keshav ◽  
SA Santhosh Kumar ◽  
Sanjeev Balaji Pai
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Aneurysmal Bone Cyst ◽  
Rare Case ◽  
Bone Cyst ◽  
Review Of Literature ◽  
Rare Case Report

scholarly journals Adnexal Tumor-Related Neurobehavioral Alterations: A Rare Case Report

2020 ◽  
Vol 2020 ◽  
pp. 1-3
Author(s):  
Gabriel Ferrante Abou Murad ◽  
Francisco Faria Hatanaka ◽  
Tamires de Menezes França ◽  
Maria Gabriela Baumgarten Kuster Uyeda ◽  
Manoel João Batista Castello Girão ◽  
...  
Keyword(s):  
Case Report ◽  
Health Service ◽  
Rare Case ◽  
Adnexal Mass ◽  
Late Onset ◽  
Clinical Manifestations ◽  
Ovarian Mass ◽  
Rare Case Report ◽  
Adnexal Tumor ◽  
Adnexal Tumors

Associations between neuropsychotic changes and oncologic disease are often described as late-onset symptoms, secondary to the instituted treatment. However, neurocognitive symptoms as a clinical manifestation of adnexal tumors are still little discussed, despite the importance of these in the gynecology practice. In this article, we present a case of adnexal mass whose first clinical manifestations were neuropsychiatric alterations. Such changes led the patient to seek our health service, and after diagnosis and treatment of the ovarian mass, the patient presented remission of the symptoms.

scholarly journals Nine-segment laminectomy is safe for the resection of a schwannoma extending from C-2 to T-3: a rare case report

2020 ◽  
Vol 29 (3) ◽  
pp. 326-31
Author(s):  
Mohamad Saekhu ◽  
Nuryati Chairani Siregar ◽  
Kevin Gunawan ◽  
Setyo Widi Nugroho
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Rare Case ◽  
Neurological Deficits ◽  
Surgical Removal ◽  
Common Complication ◽  
Rare Case Report ◽  
Normal Strength ◽  
Atypical Feature ◽  
One Year

Cervical spine schwannoma, which is long and entirely intracanal, is rare to be found. Its rarity and atypical feature leads to difficulty in diagnosing and managing cases because of the scarcity of available literature. The surgical removal of this type of schwannomas via multisegment laminectomy is a great challenge because of various risks of postoperative complications. This report describes cervical spine schwannoma that was initially was not suspected as schwannoma and was subject to surgical removal via nine-segment laminectomy. In one year after surgery, motor function returned to normal strength, no new neurological deficits occurred, and no kyphotic deformity, which is a common complication of multisegment laminectomy.

scholarly journals Minimally invasive endoscopic treatment of gastric leiomyosarcoma: A rare case report and review of literature

2021 ◽  
Author(s):  
guixiang kong ◽  
xiaolu Su ◽  
xiaojun Huang
Keyword(s):  
Case Report ◽  
Minimally Invasive ◽  
Endoscopic Treatment ◽  
Rare Case ◽  
Early Stage ◽  
Clinical Manifestations ◽  
Review Of Literature ◽  
Good Tolerance ◽  
Rare Case Report ◽  
Gastric Leiomyosarcoma

Abstract Gastrointestinal leiomyosarcoma remains relatively rare,accounting for only 1% of gastric tumors,since the use of c-kit staining was first described in 1998 to differentiate gastrointestinal stromal tumors.In this case report,we described the clinical manifestations,endoscopic features, and pathological immunohistochemical features of the gastric leiomyosarcoma.We found that endoscopic ultrasonography has great value in the diagnosis of gastric leiomyosarcoma,and that minimally invasive endoscopic treatment is safe and effective.Particularly,this case highlights that the early-stage lesions can be treated with minimally invasive endoscopic treatment with good tolerance and satisfactory clinical results.Endoscopic submucosal dissection is thus effective for treating gastric leiomyosarcoma,with promising prospects for clinical application.

scholarly journals Intramedullary Mature Teratoma of Cervical Spine in an Infant: A Rare Case Report

2014 ◽  
Vol 21 (3) ◽  
pp. 357-361
Author(s):  
Rakesh Kumar ◽  
Amit Chanduka ◽  
Devendra Purohit ◽  
Radhe Shyam Mittal ◽  
Ronyl Kaushal
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Rare Case ◽  
Pediatric Patients ◽  
Mature Teratoma ◽  
Case Series ◽  
Good Prognosis ◽  
Rare Tumor ◽  
Rare Case Report

Abstract Spinal Teratomas are rare tumor and cervical intramedullary location in infancy still rarer. Only eleven cases of cervical intramedullary teratoma in pediatric patients is reported in available literature (1, ll). We are reporting a case of an infant presenting with cervical mature teratoma with associated dysraphism, adding the next in this rare case series. Arising as a result of dysembryogenesis, these lesions by virtue of their content are difficult to diagnose preoperatively. Heterogeneous intensities on MRI produced by intralesional lipomatous and osseous elements are helpful but rarely enough to diagnose the tumor. Histology is confirmatory. Mature teratomas generally have good prognosis and a timely intervention can prevent further neurological deterioration. However a strict clinical and radiological follow up is recommended.

scholarly journals Odontogenic carcinosarcoma with dentinoid: a rare case report

2021 ◽  
Vol 49 (9) ◽  
pp. 030006052110455
Author(s):  
Xing Niu ◽  
Biying Huang ◽  
Jing Yang ◽  
Xue Qiao ◽  
Lijie Chen ◽  
...  
Keyword(s):  
Case Report ◽  
Local Recurrence ◽  
Rare Case ◽  
Tumor Resection ◽  
Clinical Manifestations ◽  
Odontogenic Tumor ◽  
Maxillary Molar ◽  
Rare Case Report ◽  
Sinus Tumor

Odontogenic carcinosarcoma is a very rare malignant odontogenic tumor, characterized by malignant epithelial and mesenchymal components. Studies have reported several cases of odontogenic carcinosarcoma, mainly in the upper and lower jaws, with malignant clinical manifestations. Herein, we present the case of a 58-year-old woman with odontogenic carcinosarcoma with dentinoid in the left maxilla. The invasion range was large, and the left maxillary molar was missing. Histology revealed odontogenic carcinosarcoma with bidirectional differentiation characteristics and comprising three components: malignant epithelium, malignant interstitium, and dentinoid. The patient subsequently underwent nasal endoscopic sinus tumor resection, and she recovered well after surgery. After a strict 4-year follow-up, to date, there are still no signs of disease or local recurrence. To our knowledge, this is the first reported case of odontogenic carcinosarcoma with dentinoid. Our study describes the clinical, morphological, and immunohistochemical characteristics of this case, and distinguishes it from related diseases.

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