Abstract:Review of the literature indicates that the optimal first line of treatment is high-dose corticosteroids. Surgery is indicated if the lesion fails to respond. Radiotherapy is indicated if complete resection is not feasible.
“…Autoimmunity has also been considered as an etiological factor. Chronic infection or inflammation leading to differentiation of plasma cells is another theory [1,2,5,7]. In our case, the history of tuberculous lymphadenitis (chronic granulomatous disease), although treated and cured maybe considered as a trigger based on the chronic inflammatory theory.…”
Section: Discussionmentioning
confidence: 78%
“…Keen et al suggested perineurofibromatosis and Du Vuysere et al suggested perineural invasion as the causative pathogenesis for neural symptoms of IMT. Our patient presented with hemifacial pain and ptosis which can be attributable to infraorbital nerve and oculomotor nerve involvement by the tumor [1,3,5,6,8,9].…”
Section: Discussionmentioning
confidence: 86%
“…Antiactin antibody positivity denotes its origin in the muscle. It is immunohistochemically negative to CD68, keratin, desmin, S-100, and caldesmon [1,3,5,6,9].…”
Section: Discussionmentioning
confidence: 99%
“…The common sites of occurrence are the abdomen and pelvis. However, it can occur in the peritoneum, central nervous system, bone, and uterus [2][3][4][5][6]. In the head and neck region, the most common site of occurrence is the orbit.…”
Section: Discussionmentioning
confidence: 99%
“…vocal folds, oral cavity, and oropharynx, nasopharynx, parapharyngeal space, and paranasal sinuses [2,3,5]. It does not occur in a specific age group, although literature reveals a median age group of 47.4 years for the occurrence.…”
Inflammatory myofibroblastic tumor (IMT) is a benign disorder of locally aggressive nature. It is an indolent tumor with a slowly progressive course and varied manifestation presenting with a wide range of clinical manifestations depending on the site of origin. We present a case of IMT in the maxillary sinus presenting with hemifacial pain, oculomotor palsy and ptosis which was successfully treated with endoscopic local excision and oral steroid therapy.
“…Autoimmunity has also been considered as an etiological factor. Chronic infection or inflammation leading to differentiation of plasma cells is another theory [1,2,5,7]. In our case, the history of tuberculous lymphadenitis (chronic granulomatous disease), although treated and cured maybe considered as a trigger based on the chronic inflammatory theory.…”
Section: Discussionmentioning
confidence: 78%
“…Keen et al suggested perineurofibromatosis and Du Vuysere et al suggested perineural invasion as the causative pathogenesis for neural symptoms of IMT. Our patient presented with hemifacial pain and ptosis which can be attributable to infraorbital nerve and oculomotor nerve involvement by the tumor [1,3,5,6,8,9].…”
Section: Discussionmentioning
confidence: 86%
“…Antiactin antibody positivity denotes its origin in the muscle. It is immunohistochemically negative to CD68, keratin, desmin, S-100, and caldesmon [1,3,5,6,9].…”
Section: Discussionmentioning
confidence: 99%
“…The common sites of occurrence are the abdomen and pelvis. However, it can occur in the peritoneum, central nervous system, bone, and uterus [2][3][4][5][6]. In the head and neck region, the most common site of occurrence is the orbit.…”
Section: Discussionmentioning
confidence: 99%
“…vocal folds, oral cavity, and oropharynx, nasopharynx, parapharyngeal space, and paranasal sinuses [2,3,5]. It does not occur in a specific age group, although literature reveals a median age group of 47.4 years for the occurrence.…”
Inflammatory myofibroblastic tumor (IMT) is a benign disorder of locally aggressive nature. It is an indolent tumor with a slowly progressive course and varied manifestation presenting with a wide range of clinical manifestations depending on the site of origin. We present a case of IMT in the maxillary sinus presenting with hemifacial pain, oculomotor palsy and ptosis which was successfully treated with endoscopic local excision and oral steroid therapy.
An abnormal clonal plasma cell proliferation with Russell bodies is rare in chronic inflammatory reactions in adult patients. We describe the first case of light chain restricted Russell body accumulation within germinal centers of lymphoid follicles of the tonsil in a child. This should not be confused with a neoplastic process.
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