Focusing on the Medicine in Dental Medicine
In: Special care in dentistry: SCD, Band 36, Heft 2, S. 59-59
ISSN: 1754-4505
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In: Special care in dentistry: SCD, Band 36, Heft 2, S. 59-59
ISSN: 1754-4505
In: Special care in dentistry: SCD, Band 36, Heft 1, S. 39-42
ISSN: 1754-4505
ABSTRACTSalivary gland malignancy (SGM) can affect both major and minor glands and manifests clinically with various presentations. The most common type of SGM is mucoepidermoid carcinoma (MEC), which has been previously reported to be associated with symptomatology associated with temporomandibular disorders (TMD). This case report describes a patient with an aggressive form of MEC of the parotid gland that was initially diagnosed as TMD. In addition, the patient's MEC was diagnosed emergently based on development of acute clinical symptomatology. To the best of our knowledge, emergency route diagnosis of MEC affecting the parotid gland has not been previously reported in the literature.
In: Special care in dentistry: SCD, Band 28, Heft 6, S. 243-253
ISSN: 1754-4505
ABSTRACTMuscular dystrophies (MD) are a heterogeneous group of inherited neuromuscular disorders characterized by muscle necrosis and progressive muscle weakness. It is important for oral healthcare providers to be familiar with MD as special considerations are necessary to provide appropriate and safe dental care for these medically complex patients. This article briefly reviews the more common types of MD, namely, Duchenne MD, Becker MD, Emery‐Dreifuss MD, facioscapulo–humeral MD, limb‐girdle MD, oculopharyngeal MD, and myotonic dystrophy. Aspects of their epidemiology, pathophysiology, clinical presentation, diagnosis, and medical management as well as oral health considerations are discussed.
In: Special care in dentistry: SCD, Band 40, Heft 4, S. 393-394
ISSN: 1754-4505
In: Special care in dentistry: SCD, Band 40, Heft 5, S. 418-430
ISSN: 1754-4505
AbstractSystemic sclerosis (SSc), also known as scleroderma, is an autoimmune disease of unknown origin characterized by an uncontrolled inflammatory process resulting in fibrosis of the skin, internal organs and vasculopathy. Manifestations of SSc are heterogenous and can include pulmonary, cardiac, neural, renal, muscular, cutaneous and orofacial complications. Recent scientific advances have led to a better understanding of disease etiopathogenesis and the development of a new classification system. Therapeutic management is often multidisciplinary and targeted toward the affected organs. Oral health care providers (OHCPs) should be familiar with SSc, particularly as it relates to its impact on the orofacial region and modifications to delivery of oral health care for patients with this condition.
In: Special care in dentistry: SCD, Band 40, Heft 6, S. 616-617
ISSN: 1754-4505
In: Special care in dentistry: SCD, Band 40, Heft 5, S. 519-524
ISSN: 1754-4505
AbstractOrofacial pain (OFP) disorders affect the maxillofacial complex and typically involve other locations in the head and neck. Common etiologies of OFP disorders include odontogenic sources, temporomandibular disorders, neuropathic pain, chemosensory disorders, and headaches. Less commonly, benign and malignant neoplasms can be associated with OFP complaints. Patients with OFP symptoms require a thorough evaluation and are often referred to additional healthcare providers for interprofessional management. In those OFP patients whose symptoms do not respond to conventional treatment(s), whose symptoms change over time, or who report positive responses to review of systems questions that suggest more extensive involvement, further investigation is warranted. To the best of our knowledge, this is the first case report of nasopharyngeal extramedullary plasmacytoma, a localized malignant neoplasm, associated with persistent OFP.
In: Special care in dentistry: SCD, Band 38, Heft 3, S. 150-154
ISSN: 1754-4505
ABSTRACTTemporomandibular disorder (TMD) is prevalent in special needs patients. Clinical examination of the temporomandibular joint (TMJ) complex and imaging in this patient population can be challenging due to patient disposition and cooperation. We report a case of a 29‐year‐old male with neurologic and behavioral special needs who required advanced maxillofacial imaging for a suspected TMD under general anesthesia, which has not been reported previously. This article intends to serve as a resource for health care providers who may encounter similar clinical situations.
In: Special care in dentistry: SCD, Band 24, Heft 2, S. 65-69
ISSN: 1754-4505
ABSTRACTAcute myelogenous leukemia (AMU is a hematologic disorder that is characterized by an abnormal proliferation of immature myeloid cells. Granulocytic sarcomas are clusters of leukemic myeloid cells that may develop as a result of AML. Oral manifestations of AML are common and often involve enlargements of the gingiva and/or mucosal tissue from direct leukemia cell infiltration. We describe the case history of a 50‐year‐old man who had an ulcera‐tive lesion of the oral mucosa that was determined to be a granulocytic sarcoma of AML‐M0 subtype. The combination of both the subtype and clinical presentation of the leukemia makes this presentation unusual, and to the best of our knowledge, of a type that has not been previously reported in the literature.
In: Special care in dentistry: SCD, Band 23, Heft 3, S. 108-110
ISSN: 1754-4505
ABSTRACTTreatment options are limited for patients with relapsed acute myelogenous leukemia (AML), particularly when the disease is refractory to standard cytotoxic chemotherapy. Targeted drug therapy offers the advantage of delivering higher doses of non‐cross‐resistant chemotherapy with potentially less systemic toxicity. Gemtuzumab ozogamicin (Mylotarg, Wyeth‐Ayerst Laboratories) is an immunoconjugate that consists of humanized anti‐CD 33 antibody linked to the potent anti‐tumor antibiotic calicheamicin and has been an effective therapy for some patients with relapsed AML. However, the overall utility of gemtuzumab ozogamicin is not well defined. For instance, it is not known how well this antibody will target extramedullar/ disease. This article reports gemtuzumab treatment of refractory AML in a 32–year‐old man. At the time of recurrence, his bone marrow was hypoplastic and without leukemia, but the condition progressed resulting in marked leukemic infiltration of the oral mucosa. This case history raises the possibility that leukemic sanctuary sites may exist, and that monoclonal antibody therapy may have sub‐optimal activity in non‐medullary sites of disease.