Triplicity—Threefold of Skull Base Tumor—Atypic Meningioma Sphenoidal Wing Left, Low-Grade Olfactory Neuroblastoma of Sphenoidal Sinuses, Neurinoma N VIII. SIN. Very Rare Case Report

Endometrial stromal sarcoma (ESS) is a rare and challenging type of endometrial tumor, constituting only about 0.2% of all uterine malignancies and occurring in women 42–58 years of age. ESS is usually misdiagnosed as leiomyoma. They both have nonspecific symptoms, which makes the diagnosis of ESS difficult to achieve. As the ESS is infrequently encountered, optimal management is quite debatable. Here, we report a rare case of a 22-year-old Syrian female who presented with abnormal uterine bleeding; the preoperative diagnosis suggested leiomyoma while histopathological and immunohistochemical studies confirmed the diagnosis of LG-ESS stage IIA. Therefore, the treatment plan was shifted from a conservative myomectomy to a total hysterectomy with both adnexa. The aim of this case report is to draw attention to this uncommon tumor at young age of patients as well as to have awareness of the necessity to suspect this diagnosis especially with the presentation of rapid enlargement of uterine leiomyoma.

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Burkitt's Lymphoma of Anterior Skull Base associated with Acute Loss of Vision: A Rare Case Report

Clinical Rhinology An International Journal ◽

10.5005/jp-journals-10013-1187 ◽

2014 ◽

Vol 7 (1) ◽

pp. 28-30

Author(s):

Varsha Varshney ◽

Gaurav Gupta ◽

Mohnish Grover ◽

Vikas Devra

Keyword(s):

Case Report ◽

Skull Base ◽

Rare Case ◽

Malignant Neoplasm ◽

Complete Recovery ◽

Burkitt’S Lymphoma ◽

Anterior Skull Base ◽

Burkitt's Lymphoma ◽

Loss Of Vision ◽

Rare Case Report

ABSTRACT Burkitt's lymphoma is a malignant neoplasm rarely found in paranasal sinuses and skull base. We report a rare case of Burkitt's lymphoma of anterior skull base associated with acute loss of vision. A 10 years old boy presented with history of headache, diminution of vision in right eye since 15 days. Biopsy showed diffuse NHL of Burkitt's type. After treatment with chemotherapy there was complete recovery in vision. How to cite this article Gupta G, Devra V, Grover M, Varshney V. Burkitt's Lymphoma of Anterior Skull Base associated with Acute Loss of Vision: A Rare Case Report. Clin Rhinol An Int J 2014;7(1):28-30.

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A Rare Case Report of Primary Low-Grade Endometrial Stromal Sarcoma (LGESS) of Ovary Infiltrating Bladder

Indian Journal of Gynecologic Oncology ◽

10.1007/s40944-016-0066-0 ◽

2016 ◽

Vol 14 (3) ◽

Author(s):

Senthil Kumar Ravichander ◽

Ajay Krishna Boralkar ◽

Neha Deepak Borde ◽

Amol Rangnath Jadhav ◽

Jyothi Sachin Mukhedkar

Keyword(s):

Case Report ◽

Rare Case ◽

Endometrial Stromal Sarcoma ◽

Low Grade ◽

Stromal Sarcoma ◽

Rare Case Report

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A maxillary ameloblastic fibrosarcoma tumor: a rare case report from Syria

Journal of Surgical Case Reports ◽

10.1093/jscr/rjaa255 ◽

2020 ◽

Vol 2020 (8) ◽

Author(s):

Amjad Soltany ◽

Ghazal Asaad ◽

Rami Daher ◽

Mouhannad Dayoub ◽

Ali Khalil ◽

...

Keyword(s):

Case Report ◽

Soft Tissue ◽

Rare Case ◽

Soft Tissue Sarcomas ◽

Surgical Excision ◽

Low Grade ◽

Rare Case Report ◽

Ameloblastic Fibrosarcoma ◽

The Right

Abstract Ameloblastic fibrosarcoma (AFS) is a rare, aggressive malignant odontogenic tumor. AFS is seen most frequently in second and third decades of life. We are reporting a case of a low grade AFS in a 21-year-old male complaining of a painless swelling in the right side of the maxilla. The patient was treated with surgical excision followed by radiotherapy, which is considered the most effective approach for most of soft tissue sarcomas. AFS has a high-reported recurrence rate (up to 37%); therefore, long-term surveillance for recurrence is crucial.

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Olfactory neuroblastoma resection through endoscopic endonasal approach: A rare case report

Annals of Medicine and Surgery ◽

10.1016/j.amsu.2022.103242 ◽

2022 ◽

pp. 103242

Author(s):

Yogi Putra Adhi Pradana ◽

Budi Sutikno

Keyword(s):

Case Report ◽

Rare Case ◽

Olfactory Neuroblastoma ◽

Endoscopic Endonasal Approach ◽

Endonasal Approach ◽

Endoscopic Endonasal ◽

Rare Case Report

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Low-grade central osteosarcoma of the mandible clinically mimicking a benign fibro-osseous lesion: A rare case report

Dental, Oral and Maxillofacial Research ◽

10.15761/domr.1000328 ◽

2020 ◽

Vol 6 (1) ◽

Author(s):

James P. Arnold ◽

Christopher J. Smith ◽

Karen E. González Torres ◽

Andrew C. Jenzer

Keyword(s):

Case Report ◽

Rare Case ◽

Low Grade ◽

Osseous Lesion ◽

Rare Case Report

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Bladder Chondrosarcoma in A Male: A Rare Case Report

Folia Medica Indonesiana ◽

10.20473/fmi.v57i3.25208 ◽

2021 ◽

Vol 57 (3) ◽

pp. 256

Author(s):

Muhammad Husni Tamrin ◽

Wahjoe Djatisoesanto

Keyword(s):

Case Report ◽

Soft Tissue ◽

Soft Tissue Sarcoma ◽

Rare Variant ◽

Rare Case ◽

Bladder Tumor ◽

Histopathological Examination ◽

Low Grade ◽

Lower Abdomen ◽

Rare Case Report

Chondrosarcoma is a rare variant of bladder tumor and one of the rare types of soft tissue sarcoma. This case happened on a 36-year-old male who complained of lumps in his lower abdomen, accompanied by difficulties in passing urine and painful urination, without hematuria. We performed TURBT and histopathological examination showed low-grade chondrosarcoma. The patient was diagnosed with low-grade bladder chondrosarcoma. The patient was treated for chemotherapy and radiotherapy. However, after undergoing one cycle of chemotherapy, the patient refused to continue the therapy.

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