Search

• A variety of methods for abdominal wall closure have been described. • Closure of a defect by myocuteous thigh flap is a viable option. • In this report, bilateral anterolateral myocutaneous thigh flaps has been discussed. Closure of the abdominal wall defect by myocuteous thigh flap is an option. The aim of this paper is to report a case of abdominal wall defect covered by bilateral anterolateral myocutaneous thigh flap. A 45-year-old female presented with a large defect in the anterior abdominal wall. It was decided to cover the wound with bilateral anterolateral myocutaneous thigh flap as the defect was so large to be filled with a single flap. Under general anesthesia, a flap was elevated lateral to a line joining mid inguinal point to the lateral epicondyle, the flap was rotated under inguinal skin and sutured to the defect. The procedure was repeated for the contralateral side two weeks later. Lower abdominal wall defects can be reconstructed by the use of the combined technique of sublay technique, intraperitoneal mesh placement, pedicled great omentum flap and rotation skin graft, also tensor fascia lata has been proven to be a safe and versatile flap. Bilateral anterolateral myocutaneous thigh flap is practical whenever indicated. It is best suited for covering of the lower abdominal defects. [ABSTRACT FROM AUTHOR]

• Sacrococcygeal PNS is the commonest variant of the condition. • However, it can occur in other areas like umbilicus, hand, scalp intermammary, suprapubic, nose, etc. • Infra mammary PNS is an extremely rare condition, with no previous report. • This study aims to present and discuss a case of PNS occurring in both infra mammary regions. Pilonidal sinus (PNS) is a chronic inflammatory perianal disorder that rarely occurs outside sacrococcygeal region. The aim of this study is to report an extremely rare case of bilateral inframammary PNS with brief literature review. A 25-year-old female presented with a discharging sinuses in both inframammary region for two years. Examination showed multiple discharging sinuses with several centimeters of induration and tenderness. Under general anesthesia, complete excision of the sinuses with primary closure done. Histopathological examinations showed chronic foreign body granuloma surrounding hair shaft pictures consistent with PNS. Inframammary PNS has never been reported in the literature. As with intermammary PNS, in this case also it is associated with obesity and large breasts with tight brassieres. Diagnosis is usually clinical. In contrast to sacrococcygeal PNS, operation under general anesthesia is main treatment modality. Pilonidal sinus of inframammary region is an extremely rare condition. High index of suspicion is required for diagnosis. Excision with primary closure is the definitive therapy. [ABSTRACT FROM AUTHOR]

Acinar cell carcinoma (ACC) of the pancreas is a rare neoplasm which is mostly diagnosed in late adulthood. This study aims to report an incidental finding of ACC in a child who was treated successfully with operation. A 9-year-old male presented with signs of delayed growth. Physical examination revealed a swelling in the left upper abdomen, which was shown to be a pancreatic tumor on a CT scan. Total surgical excision of the neoplasm was performed and the histopathology report confirmed the diagnosis of ACC. Pancreatic ACC is very rarely reported in children and its signs and symptoms are non-specific. Its diagnosis needs a high index of suspicion and CT scan is a good imaging modality for detection. Resectable tumors are best managed with complete removal of the cancer, while unresectable neoplasms can be treated with chemotherapy. However, treatment guidelines and prognosis of pancreatic ACC are not clear in pediatric age groups due to scarcity of reports. Accidental finding of ACC involving the body and tail of the pancreas is extremely rare in children. Early detection and proper management provide an excellent outcome. [ABSTRACT FROM AUTHOR]

The synchronous development of a medullary and papillary carcinoma as two different tumors has only been reported very rarely. The aim of the current report is to describe an extremely rare occurrence of medullary carcinoma, papillary microcarcinoma, and Hashimoto thyroiditis. A 53-year-old man presented with a right-sided neck mass. Ultrasound showed a well-defined nodule in the right mid third with microcalcification and increased nodular vascularity associated with multiple right-sided cervical lymphadenopathy. The histopathological examination showed multifocal medullary carcinoma with incidental finding of unifocal papillary microcarcinoma conventional type on the left side. Additional pathology of Hashimoto thyroiditis with a small intra-thyroidal parathyroid gland in the left thyroid gland. The procedure went perfectly and the patient was discharged home without any difficulties. Synchronous existence of these two neoplasms can occur in two forms: distinct medullary carcinoma and papillary carcinoma isolated by normal thyroid tissue, or mixed medullary and follicular-derived thyroid carcinoma, in which single or multiple lesions show morphology and immunoreactivity for both medullary carcinoma and follicular-derived carcinoma. The synchronous coexistence of papillary microcarcinoma, medullary carcinoma, and Hashimoto's thyroiditis is an uncommon thyroid condition. • Thyroid malignancies are less common than other types of cancer. • The interactions between medullary and papillary carcinomas are of particular interest. • Synchronous development of medullary and papillary carcinoma has been reported very rarely. • In this paper, the occurrence of Hashimoto thyroiditis with papillary carcinoma and medullary carcinoma is reported. [ABSTRACT FROM AUTHOR]