Soft-Tissue Chondroma in the Right Hallux: A Case Report

2019 ◽  
Vol 109 (6) ◽  
pp. 451-454
Author(s):  
Xingpei Hao ◽  
Joon Yim ◽  
Chenfeng Qi ◽  
Gene Mirkin
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Physical Examination ◽  
Benign Tumor ◽  
Proximal Phalanx ◽  
Surgical Excision ◽  
Cartilaginous Matrix ◽  
Rare Benign Tumor ◽  
The Right ◽  
Hands And Feet

Soft-tissue chondroma is a rare, benign tumor. It is predominantly found in the hands and feet, but rarely in the toes. In this article, we report a digital soft-tissue chondroma that presented as a painful nodule of 5 years' duration in a 67-year-old man. Physical examination revealed a round, solid, movable nodule measuring 7 mm in diameter. Radiographs showed faint linear calcifications in the nodule under the right hallux proximal phalanx neck. The mass was completely excised, and pathologic observation revealed a mass composed of mature chondrocytes in a cartilaginous matrix, consistent with a chondroma. Even though this is a benign tumor, it needs to be differentiated from other tumors, including schwannoma, leiomyoma, chondrosarcoma, and others. Surgical excision is the preferred treatment.

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

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.

scholarly journals Odontogenic Myxoma of the Maxilla - A Case Report

2019 ◽  
Vol 6 ◽  
Author(s):  
Adil Eabdenbtsen ◽  
Mohammed Mouzouri ◽  
Ahlam Bellouchi ◽  
Noureddine Oulali ◽  
Mohammed Bouziane ◽  
...  
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Benign Tumor ◽  
High Rate ◽  
Odontogenic Myxoma ◽  
Radical Treatment ◽  
Rare Benign Tumor ◽  
The Right

Introduction : The odontogenic myxoma is a rare benign tumor of the maxilla, whose clinical and radiological manifestations are variable and nonspecific and can be confused with other radiolucent lesions. Its origin would be the embryonic mesenchyme of the dental follicle.Case report : We report the case of odontogenic myxoma of the right maxilla, discovered by chance in a 25 year old patient. Clinically, the patient had painless, firm on palpation, swelling of the right maxilla, impeding chewing and speech. Facial CT-scan showed an expansive osteolytic process blowing the right maxilla off. A biopsy was in favor of an odontogenic myxoma. The diagnosis was based on clinical, radiological and especially anatomopathological arguments.Conclusion : The local aggressiveness of the odontogenic myxoma and its high rate of recurrence justify a radical treatment beyond the lesion’s boundaries and thus imply a postoperative repair.

scholarly journals A CASE REPORT OF FEMUR OSTEOCHONDROMA IN 22 YEARS OLD FEMALE PATIENT

2020 ◽  
Vol 8 (10) ◽  
pp. 1263-1267
Author(s):  
Abdulrahman M. Bin Mohi ◽  
◽  
Ahmed A. Alzahrani ◽  
Bashar R. Reda
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Proximal Femur ◽  
Conflict Of Interest ◽  
Distal Femur ◽  
Tumor Resection ◽  
Surgical Excision ◽  
Low Grade ◽  
The Right ◽  
Hands And Feet

Chondromais considered a nonmalignant tumor that composed of mature hyaline cartilage and commonly occur in hands and feet. Overall incidents show that females are predominant comparing to males with evenly distributed range of ages. Multiple chondromas have to be differentiated from osteochondroma and chondrosarcoma. This paper reports three different types of lesions in one patient.Osteochondroma or exostosis is the most common benign tumor of the skeleton. It is a developmental osseous anomaly, which arises from exophytic outgrowth on bone surfaces characteristically. Osteochondroma account for about 12% of bone tumors. Here, we have described a 22 years old female patient with left knee joint pain and swelling of the left distal femur with limited movements. The incisional biopsy of the left distal femur identified low-grade chondrosarcoma and chondroma after histopathology. This underwent one-stage surgical excision of the tumor with a posterior approach and tumor resection from the femur. After surgery, an unusual pain appears in the right hip joint during the post-operative period.Machine resonance imaging (MRI), and X-ray of pelvis help to diagnose thewell-differentiated chondrosarcoma and chondroma. This was a case of osteochondroma in the right proximal femur, chondroma like lesion in the left proximal femur and chondrosarcoma in the left distal femur. Ethical consideration: Written informed consent was obtained from the patient for publication of this case report and accompanying images. Conflict of interest: There is no conflict of interest.

scholarly journals Piloleiomyoma Presented by Multiple Cutaneous Nodules: a Case Report

2020 ◽  
Vol 12 (4) ◽  
pp. 157-161
Author(s):  
Lala Cahangirova ◽  
Jamal Musayev
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Treatment Option ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Smooth Muscle Contraction ◽  
Punch Biopsy ◽  
Channel Blockers ◽  
Rare Benign Tumor ◽  
Adrenergic Blockers

Abstract Introduction. Piloleiomyoma is a rare benign tumor which is caused by erector pili muscle and makes up 5% of all leiomyomas. They can be solitary and multiple. Multiple lesions still pose challenges for clinicians since their treatment option is very limited. Case report. We report a case of a 25-year-old male patient who had painful papules and nodules on the neck and chest for three years. Multiple red-brown papules and nodules in the skin of regio mammaria dextra and regio submandibularis on the left were seen on physical examination. Histopathological examination of punch bi-were seen on physical examination. Histopathological examination of punch biopsy sample revealed well-circumscribed nodule composed of spindle cells. The case was reported as cutaneous leiomyoma (piloleiomyoma). The patient was given 5 mg/day amlodipin and kept under control. Conclusion. The ideal treatment option for piloleiomyoma is surgical excision, but the problem with that treatment is that the lesions have tendency to recur. Medicamentous therapy plays a limited role; however, calcium-channel blockers and α-adrenergic blockers may help in palliating or eliminating associated pain through inhibition of smooth muscle contraction.

scholarly journals Mastoid Osteoma

2019 ◽  
Vol 27 (2) ◽  
pp. 167-170
Author(s):  
Rabi Hembrom ◽  
Rupam Sinha ◽  
Amit Chakrabarti ◽  
Indranil Sen
Keyword(s):  
Case Report ◽  
Postoperative Period ◽  
Benign Tumor ◽  
Surgical Excision ◽  
Complete Removal ◽  
The Right ◽  
Mastoid Region

Introduction Osteoma of the mastoid region is an uncommon benign tumor of bone. Osteomas may occur in the external auditory canals but are reported to be very rare in the mastoid region, with about 150 cases reported in literature. Case Report A 20-year-old man presented with painless lump behind the right ear since last 2 years. On examination a 3x3 cm tumour was present in the right post-auricular region. HRCT scan showing hyper-attenuating area close to the right mastoid cortex, measuring approximately 3x3cm, spherical, with cleavage areas between the tumour and the mastoid external cortex. Surgical excision was performed on cosmetic grounds. Postoperative period was uneventful. Discussion Osteoma over the mastoid region is rare and mainly asymptomatic with excellent prognosis after complete removal of the lesion.

scholarly journals UNE LOCALISATION RARE DUN SCHWANNOME ORBITAIRE A RARE LOCALIZATION OF AN ORBITAL SCHWANNOMA

2020 ◽  
Vol 8 (9) ◽  
pp. 941-944
Author(s):  
Zahra Sayad ◽  
◽  
Bouchra Dani ◽  
Malik Boulaadas
Keyword(s):  
Iliac Crest ◽  
Benign Tumor ◽  
Histological Analysis ◽  
Surgical Excision ◽  
Ocular Motility ◽  
Iliac Crest Graft ◽  
Complete Surgical Excision ◽  
Operative Specimen ◽  
Rare Benign Tumor ◽  
The Right

Introduction: The infraorbital schwannoma or neuroma is a rare benign tumor of the orbit. Its clinical and radiological presentation is not very specific. Its diagnosis is essentially histological. Observation: We report the case of a 46-year-old woman, diabetic under treatment, consulting for an irreducible, non-axial and non-pulsatile exophthalmos. Clinical examination of the left eye found visual acuity corrected to 8/10 without limitation of ocular motility or diplopia. The examination of the right eye is unremarkable.The orbital CT objectified a mass measuring 25.3mm × 13.8mm, homogeneous of the floor of the left orbit, pushing the eyeball up and out. The orbital floor was pushed inferiorly by the mass however, its integrity was preserved. Tumor excision was performed via the sub-ciliary cutaneous incision with reconstruction of the floor by an iliac crest graft. The histological analysis allowed us to have a definite diagnosis of schwannoma. Conclusion:The schwannoma is a rare tumor of the orbit. Its diagnosis is established solely by anatomopathological study of the operative specimen. Its treatment is based on a complete surgical excision to avoid any recurrence.

scholarly journals Myofibroma of the Gingiva: A Rare Case Report and Literature Review

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Vaishali Narayen ◽  
Syed Afroz Ahmed ◽  
Charu Suri ◽  
Shahela Tanveer
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissues ◽  
Surgical Excision ◽  
Soft Tissue Tumors ◽  
Immunohistochemical Examination ◽  
Internal Organs ◽  
Rare Case Report ◽  
Rare Benign Tumor ◽  
Clinical Differential Diagnosis

Myofibromas are benign uncommon fibroblastic tumors of the soft tissue, bone, or internal organs affecting all ages. These lesions histopathologically may mimic many other soft tissue tumors of the oral cavity such as spindle cell tumors of neurogenic and smooth muscle cell origin, thus leading to misdiagnosis and mistreatment. This case report describes a rare benign tumor, which presented as a soft tissue swelling on posterior gingiva. Surgical excision of the lesion was carried out under local anaesthesia. Histopathologic and immunohistochemical examination confirmed the diagnosis of myofibroma. Myofibroma should be included in the clinical differential diagnosis of masses of the oral soft tissues; however immunohistochemical examination is essential to establish an accurate diagnosis.

scholarly journals Adenomatoid Tumor of Epididymis-A Case Report

KYAMC Journal ◽  
2018 ◽  
Vol 9 (3) ◽  
pp. 141-145
Author(s):  
Ashraf Uddin Mallik ◽  
Md Mostafizur Rahman ◽  
Uttam Karmaker ◽  
Baikali Ferdous
Keyword(s):  
Case Report ◽  
Fine Needle Aspiration ◽  
Benign Tumor ◽  
Needle Aspiration ◽  
Adenomatoid Tumor ◽  
Aspiration Cytology ◽  
Fine Needle ◽  
Rare Benign Tumor ◽  
Needle Aspiration Cytology ◽  
The Right

Adenomatoid tumor is a very rare benign tumor of mesothelial origin. It is very difficult to distinguish carcinoma from an adenomatoid tumor. This is a report of a case of an adenomatoid tumor of the right epididymis of a man of 38-year-old who came to Urology OPD with pain and palpable swelling on the right testis. He also complaints of severe burning during ejaculation. We diagnose the case by ultrasonogram (USG) and Fine Needle Aspiration Cytology (FNAC). Right epididymectomy has done and histopathology revealed adenomatoid tumor. As the tumor is very rare, the case is to report for its clinical entity.KYAMC Journal Vol. 9, No.-3, October 2018, Page 141-143

scholarly journals Giant vulva fibroma presenting as a genital mass: a case report

2020 ◽  
Vol 21 (2) ◽  
pp. 1-6
Author(s):  
Edgar Ndaboine ◽  
Dismas Matovelo ◽  
Arnold Itemba ◽  
Cosmas Mbulwa
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Spinal Anesthesia ◽  
Surgical Excision ◽  
Well Being ◽  
Hormonal Changes ◽  
Case Presentation ◽  
Limited Mobility ◽  
The Right ◽  
Unusual Finding

Introduction: Even though vulva fibroma is rare, it is among the solid tumors of the vulva. Its cause is unknown although it has been associated with physiological hormonal changes. We report a patient with a unique vulva fibroma which has grown to the extent of interfering with her gait and urination. Case presentation: A 22-year-old woman presented with a genital mass which had been present for the duration of 2 years and felt embarrassed to report to the hospital early as the growth was in the genital area, with the perception of it being a sexually related illness, despite having not yet started engaging in sexual activity. On physical examination, a palpable pendulous mass of about [30 x 22] cm was seen originating from the right labia and extending to the right perineum. The mass was firm, nodulated, non-tender and had limited mobility. Surgical excision was performed under spinal anesthesia. Histologically, features suggestive of mixoid fibroma were reached after the mass was excised.  No recurrence has been observed. Conclusion: Clinicians should be aware of this rare disease which can be associated with recurrence if there is incomplete excision. Again, the unusual finding of the genital mass can be very embarrassing to the patient affecting her psychosocial well-being. It needs to be treated immediately upon diagnosis.  

An Invasive Hemolymphangioma of the Pancreas in a Young Woman

2019 ◽  
Vol 21 (10) ◽  
pp. 798-800 ◽  
Author(s):  
Zhijun Zhang ◽  
Qinghong Ke ◽  
Weiliang Xia ◽  
Xiuming Zhang ◽  
Yan Shen ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Young Woman ◽  
Benign Tumor ◽  
Abdominal Distension ◽  
Accurate Diagnosis ◽  
Cystic Tumor ◽  
Rare Benign Tumor ◽  
Radical Surgical Resection

Background: Hemolymphangioma is a rare benign tumor. To the best of our knowledge, there were only 10 reports of this tumor of the pancreas until March 2018. Case Report: Here, we reported a large invasive hemolymphangioma of the pancreas in a young woman with a complaint of abdominal distension and an epigastric mass about 3 weeks. She was found to have a huge multilocular cystic tumor at the neck and body of pancreas on computed tomography. She was eventually diagnosed with hemolymphangioma of the pancreas after operation. After 2 years of follow-up, there was no signs of recurrence. Conclusion: From our case and literature, we can conclude that hemolymphangioma of the pancreas is uncommon benign tumor, and it is hard to make an accurate diagnosis preoperatively. Radical surgical resection should be performed whenever possible. The prognosis of this disease seems good.

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