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1.
Autops. Case Rep ; 10(2): e2020156, Apr.-June 2020. tab, graf
Article in English | LILACS | ID: biblio-1131806

ABSTRACT

Hyalinizing clear cell carcinoma (HCCC), also known as clear cell carcinoma, not otherwise specified [CCC, (NOS)], is a rare minor salivary gland tumor characterized by proliferation of clear cells, organized in trabecular cords, or solid nests within loose to densely hyalinized stroma. It is considered a diagnosis of exclusion by the World Health Organization (WHO) because other salivary tumors may also have a clear cell component. Hence, there is a wide differential diagnosis. EWSR1-ATF1 gene rearrangements are fairly specific for this tumor, however, one of the recent studies have described its presence in clear cell odontogenic carcinoma (CCOC) one of its histologic mimickers. EWSR1 and CREM fusions have recently been described in these tumors but its importance is still not well described. Here we present a case of a 33-year-old woman who presented with a recurrent lesion of the soft palate. Her initial lesion was resected and diagnosed as low-grade myoepithelial tumor. Surgical margins at the time of initial resection were positive and the re-excision was recommended but the patient did not undergo surgery. Two years later, local recurrence at the same site was found and an excision was performed yielding negative margins. Histopathologic examination revealed features consistent with hyalinizing clear cell carcinoma. The patient remains disease free 1 year after the re-excision. The pathology, clinical characteristics, differential diagnosis and treatment of hyalinizing clear cell carcinoma are reviewed.


Subject(s)
Humans , Female , Adult , Salivary Gland Neoplasms/diagnosis , Carcinoma , Pathology, Clinical , Diagnosis, Differential
2.
Autops. Case Rep ; 8(1): e2018004, Jan.-Mar. 2018. ilus, tab
Article in English | LILACS | ID: biblio-905425

ABSTRACT

Teratomas are one of the most frequent tumors in the pediatric population. They occur anywhere along the midline of the body, following the course of the embryonic germ cell ridge. In the mediastinal location, they exert space occupying effects, leading to a myriad of complications, including non-immune hydrops fetalis. We describe a fatal case of an immature thymic teratoma in a neonate presenting with hydrops fetalis. This case emphasizes the importance of early diagnosis and surgical intervention in such cases.


Subject(s)
Humans , Male , Infant, Newborn , Hydrops Fetalis/diagnosis , Mediastinal Neoplasms/complications , Teratoma/complications , Autopsy , Erythroblastosis, Fetal/diagnosis , Fatal Outcome , Hydrops Fetalis/pathology , Teratoma/diagnosis , Teratoma/pathology
3.
Autops. Case Rep ; 7(4): 37-41, Oct.-Dec. 2017. ilus
Article in English | LILACS | ID: biblio-905404

ABSTRACT

Disseminated toxoplasmosis is a life-threatening disease in immunocompromised individuals. Infection is contracted from handling contaminated soil, cat litter, or through the consumption of contaminated water or food. It is the third most common lethal foodborne infection in the United States. In transplant patients, most cases occur as a result of reactivation of a latent infection resulting from immunosuppression. We present a case of disseminated toxoplasmosis diagnosed at the time of autopsy. This case emphasizes the importance of maintaining a high index of clinical suspicion and active disease surveillance in this era of sophisticated diagnostic testing.


Subject(s)
Humans , Male , Middle Aged , Opportunistic Infections/complications , Toxoplasmosis/complications , Transplant Recipients , Allografts , Autopsy , Fatal Outcome , Heart Arrest/etiology , Immunosuppression Therapy , Kidney Transplantation/adverse effects , Respiratory Insufficiency/etiology , Toxoplasmosis/diagnosis , Toxoplasmosis/pathology
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