Short Name: J Surg Case Rep
Publisher: MedDocs Publishers LLC
Although the primary pathology of Hirschsprung's disease is a congenital gut motor neuron development disorder causing functional intestinal obstruction, which is diagnosed in over 94% of cases with clinical evidence and histologic examination before children reach the age of five, the term "adult Hirschsprung's disease" is conventionally used as a clinical trend when the disease is diagnosed in an adult who is older than ten years.
Angiomyxolipoma is a rare, benign soft tissue tumor characterised by the presence of mature adipose tissue, myxoid stroma, and a prominent vascular component. This case report details the clinical presentation, histopathological features, treatment, and follow-up of a 59-year-old male patient diagnosed with angiomyxolipoma of the forehead.
Intra-abdominal neurofibromatosis is an exceedingly rare diagnosis constituting a challenge for clinicians in diagnosis and management. With only a few cases reported worldwide, there is no consensus on management protocol. Because appendiceal neurofibromas are benign, surgical excision is the main therapeutic option, and the prognosis is usually good.
Rectal prolapse is defined as entire thickness rectum protrusion past the anal sphincter. The prolapsed section of the rectum can become cancerous in rare cases. Although the exact incidence of rectal prolapse is unknown, it is a relatively uncommon condition. We present a case of rectal prolapse accompanied by neoplastic transformation.
Primary neuroendocrine tumors of the breast are an uncommon and often overlooked subtype of breast carcinoma primarily affecting postmenopausal women. These rare tumors account for approximately 2-5% of all breast cancers and are classified as well-differentiated Neuroendocrine Tumors (NETs)
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Authors
Xie Yin1*; Wu Chunyu2
1Department of Blood transfusion, People’s Hospital of Kaizhou District, Chongqing, 405419, China.
2Department of Urology, People’s Hospital of Kaizhou District, Chongqing, 405419, China.
Received: Aug 22, 2022
Accepted: Sep 16, 2022
Published Online: Sep 19, 2022
