Intraabdominal Heterotopic Ossification after appendectomy Mimicking Undescended Testicular Tumor: a rare case report and literature review
نویسنده
چکیده
Reprint requests to: Dr. Ruey-Sheng Chang Department of Medical Imaging, Chia-Yi Christian Hospital. No. 539, Jhongsiao Road, Chiayi 600, Taiwan, R.O.C. Intraabdominal heterotopic ossif ication is a rare sequela of abdominal surgery or trauma. Only a few previous reports have been described in the literature. Here, we report the case of a 20-year-old man who underwent appendectomy 3 years ago and experinced this condition. Initially, he presented with right undescended testis with a palpable mass in the right lower abdomen. Plain radiography and computed tomographic imaging showed peripheral calcified soft tissue mass. Explorative laparotomy for excision was performed and heterotopic ossification was diagnosed by pathologic findings. The characteristic imaging features of this rare entity are discussed and the literature are reviewed. Heterotopic ossification (HO) is the abnormal formation of t rue bone within extraskeletal soft t issues. Classically, many diseases shar ing this common feature were lumped into the category myositis ossificans; however, the term has fallen into disfavor because primary muscle inflammation is not a necessary precursor for such ossification and the ossification does not always occur in muscle tissue. The term HO has largely replaced myositis ossificans in the literature [1]. Mature HO closely resembles normal bone both histologically and radiologically, and thus it differs from dystrophic calcification in soft tissues, in which there is no osteoblastic activity or lamellar bone. Heterotopic ossif ication has been reported in the context of several conditions—most notably total hip arthroplasty and neurologic injuries [2, 3]. However, intraabdominal HO is a rare sequela of abdominal surgery or trauma and of unknown etiology. Here, we present a patient who experienced intraabdominal HO after appendectomy.
منابع مشابه
Ruptured Hemorrhagic Cyst of Undescended Ovary Mimicking Mucocele: A Rare Pediatric Case
Undescended ovary is a rare entity and usually presentedas a case report. It is associated with urinary and uterine anomalies. Symptomatic patients are diagnosed during surgery. Most of the patients are asymptomatic and treatment is unnecessary. They are incidentally diagnosed during infertility evaluation and treatment such as ovarian hyperstimulation studies.A 15-year-old female patient prese...
متن کاملHeterotopic Ossification around the Knee after Internal Fixation of a Complex Tibial Plateau Fracture Combined with the Use of Demineralized Bone Matrix (DBM): A Case Report
Demineralized bone matrix has been successfully commercialized as an alternative bone graft material that not only can function as filler but also as an osteoinductive graft. Numerous studies have confirmed its beneficial use in clinical practice. Heterotopic ossification after internal fixation combined with the use of demineralized bone matrix has not been widely reported. In this paper we de...
متن کاملRenal Capillary Hemangioma Mimicking Urothelial Carcinoma, A Case Report and Review of the Literature
Renal hemangioma is a rare tumor which can be capillary or cavernous. There have been less than 30 renal capillary hemangioma cases reported in the English literature. Herein we will report a case of renal hemangioma which was detected in a 74-year-old man operated with the impression of urothelial carcinoma of hilum.
متن کاملPRIMARY LOCALIZED RETROPERITONEAL AMYLOID TUMOR WITH OSSEOUS META PLASIA: CASE REPORT AND REVIEW OF THE LITERATURE
Amyloidoma or amyloid tumor is a tumor-like localized deposit of amyloid encountered occasionally in association with multiple myeloma, various chronic inflammatory diseases and primary amyloidosis. Amyloid tumors unassociated with plasmacytoma or other disease are extremely rare in soft tissues and few cases in various situations have been reported. Histologic examination discloses amorp...
متن کاملSclerosing Sertoli Cell Tumor of the Testis: Case Report and Review of the Literature
Sertoli cell tumors of the testis are extremely rare tumors with a heterogeneous pathology. Three histological variants have been described: Sertoli cell tumor not otherwise specified (NOS), large cell calcifying sertoli cell tumor and the Sclerosing Sertoli cell tumor. The sclerosing Sertoli cell tumor described herein is associated with prominent stromal sclerosis. They present as painless...
متن کامل