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1.
Int J Surg Case Rep ; 105: 108023, 2023 Apr.
Article in English | MEDLINE | ID: mdl-36958146

ABSTRACT

INTRODUCTION AND IMPORTANCE: Desmoid fibromatosis is a benign monoclonal fibroblastic tumor that was first reported in 1832 and arises from musculoaponeurotic structures. It is an uncommon tumor that can mimic breast carcinoma in both hits clinical and radiological presentation. This entity mainly affects patients in their fourth and fifth decades of life. CASE PRESENTATION: Our four patients were of young women in their 2nd and 3rd decade that consulted for masses of the breast. These lesions were suspicious for malignancy in both their clinical and radiological features despite not having any family history of breast carcinoma. CLINICAL DISCUSSION: Only histology provides the diagnosis, it is locally invasive, non-metastatic but with a high potential of recurrence and the sole treatment is complete and wide local excision with clear margins. CONCLUSION: Although it is a rare clinical scenario, the presence of an unusual breast or chest wall tumor such as a desmoid tumor should be considered when obvious breast changes and history do not correlate with routine diagnostic measures.

2.
Int J Surg Case Rep ; 99: 107598, 2022 Oct.
Article in English | MEDLINE | ID: mdl-36137430

ABSTRACT

INTRODUCTION: Gastrointestinal stromal tumors (GISTs) usually develop in the stomach and small intestine and only rarely occur in the ampulla of Vater (AV). CASE PRESENTATION: We report a case of a GIST of the AV. A 21-year-old, previously healthy woman presented with a three-month history of epigastric pain, jaundice and weight loss. The diagnosis of a tumor in the second part of the duodenum was made by the computed tomography. The patient underwent pancreatoduodenectomy, the operative specimen revealed an intermediate risk group of GIST and thus, the patient didn't take adjuvant therapy. DISCUSSION: GIST rarely develops in the duodenal ampulla region and it has no specific symptomatology. Radiological investigations play an important role in the diagnosis of Stromal Tumor of the Ampulla of Vater (STAV) mainly computed tomography because STAV has a large size in the majority of cases contrary to adenocarcinoma. CONCLUSION: The aim of this study is to report a new case of STAV combined with a systematic review of reported cases published in peer-reviewed journals.

3.
J Stomatol Oral Maxillofac Surg ; 123(5): e402-e404, 2022 10.
Article in English | MEDLINE | ID: mdl-35235881

ABSTRACT

Calcinosis is defined as a biomineralization occurring in soft tissues leading to ectopic calcification. Isolated and localised calcification in a muscle is rare, and it is called calcinosis circumscripta in opposition to calcinosis universalis wich is seen in juvenile dermatomyositis and polymyositis. According to laboratory findings and clinical history, calcinosis circumscripta can be metastatic, dystrophic or idiopathic. Masseter muscle is rarely involved. Pre-operative diagnosis of masseter idiopathic calcinosis is a challenge because of many differential diagnosis. Here, we report a case of 22 years old women presented with swelling over left middle third of her face. Clinical history, morphologic and laboratory examinations helped considering such a rare diagnosis.


Subject(s)
Calcinosis , Dermatomyositis , Adult , Calcinosis/diagnosis , Calcinosis/etiology , Calcinosis/surgery , Dermatomyositis/complications , Dermatomyositis/diagnosis , Diagnosis, Differential , Female , Humans , Masseter Muscle/pathology , Masseter Muscle/surgery , Young Adult
4.
Pan Afr Med J ; 30: 7, 2018.
Article in French | MEDLINE | ID: mdl-30123410

ABSTRACT

Breast cancer is the most common cancer among women. Prognosis depends, in large part, on the presence of metastases. Liver, skeleton and lungs are the most frequent metastatic sites, whereas genital metastases are more rare and less known. The detection of an ovarian mass in a woman with a history of breast cancer raises the question of its primary or secondary origin. The frequency of ovarian metastases reported in the literature is approximately 20-30%. However, when an ovarian mass is detected in a woman with breast cancer, primary ovarian tumor is diagnosed three times more often than a metastasis. Cervical, uterine or corporeal metastases are even more rare. They are often diagnosed late, due to their clinical latency; transvaginal ultrasound coupled with Color Doppler and Pap smear must be performed as first-line examinations knowing that their screening performance in patients with ovarian masses is deemed low. An increase in CA 15-3 and CEA tumor markers must lead clinicians to investigate for metastases, but it doesn't provide diagnostic orientation toward a specific metastatic site. Finally, only anatomo-athological examination allows certain diagnosis. We here report 3 cases of genital metastases from primary breast cancer (two patients with ovarian metastases and one patient with cervico-uterine metastasis) in order to highlight the role of accurate and regular genital examination in the monitoring of patients with breast cancer and to discuss the predictive factors for their occurrence.


Subject(s)
Breast Neoplasms/pathology , Ovarian Neoplasms/secondary , Uterine Cervical Neoplasms/secondary , Biomarkers, Tumor/analysis , Breast Neoplasms/diagnosis , Female , Humans , Middle Aged , Ovarian Neoplasms/diagnosis , Prognosis , Uterine Cervical Neoplasms/diagnosis
5.
J Neonatal Surg ; 6(2): 41, 2017.
Article in English | MEDLINE | ID: mdl-28770138

ABSTRACT

Anterior urethral valves (AUVs) is an unusual cause of congenital obstruction of the male urethra, being 15-30 times less common than posterior urethral valves. We present a case of AUV diagnosed at 24th gestational week. Ultrasonography and fetal MRI revealed hydronephrotic kidneys with ureteral duplicity, a distended bladder and perineal cystic mass which confirmed dilated anterior urethra in a male fetus. Diagnosis was confirmed postnatally by voiding cystourethrogram and surgery.

6.
Cancer Biol Med ; 14(4): 414-417, 2017 Nov.
Article in English | MEDLINE | ID: mdl-29372108

ABSTRACT

Squamous cell carcinoma (SCC) of the rectum is a rare disease. A 59-year-old man presented with SCC of the middle rectum located 10 cm from the anus. The stage of the tumor was revealed to be T3N+M0. The patient received a combined treatment with cisplatin and fluorouracil in concomitance with external radiation therapy. He then underwent an anterior resection of the rectum. The postoperative histopathological findings classified the tumor as ypT0N0 with cancer-free margins and lymph nodes. Treatment of SCC remains very challenging, and the acquisition of more consistent data is needed.

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