We reviewed 43 fine-needle aspiration biopsy (FNAB) smears with abundant extracellular mucinous material to determine whether accurate classification of mucinous lesions is achievable on FNAB: 26 had carcinoma (pure colloid carcinoma [CCA], 23; mixed CCA/invasive ductal carcinoma [IDC], 3); 17 had benign lesions on follow-up (benign MLL, 6; fibrocystic change [FCC], 6; myxoid fibroadenoma [MFA], 5). All carcinomas were identified correctly as malignant on FNAB. The initial cytologic diagnoses in benign cases were benign in 8, atypical in 8, and "suspicious" for carcinoma in 1. CCAs were moderate to markedly cellular with mild to moderate atypia and lacked oval bare nuclei. Marked nuclear atypia was confined predominantly to cases with mixed CCA/IDC. A distinct feature of CCA was thin-walled capillaries. FCCs and benign MLLs had overlapping cytologic features and showed variable cellularity and no or mild atypia. MFAs were markedly cellular with dyscohesion and variable atypia; stromal fragments and oval bare nuclei were present in every case. Mucinous lesions can be divided into 2 categories by FNAB: those that are adenocarcinomas and those that are not. CCAs have distinctive features that allow a definitive diagnosis on FNAB. Unnecessary surgery can be avoided in MFA by careful evaluation of smear characteristics. Cytologic features of FCC and MLL overlap. Owing to the documented association of MLL with carcinoma, we recommend that lesions that cannot be classified definitively as adenocarcinoma or MFA be considered for conservative excision, even in the absence of atypia.
A full-term, healthy male neonate was delivered by caesarian section to a 26-year-old primigravida woman who had a history of fever and upper respiratory tract infection. On the fourth day of life, the neonate developed a sepsis-like syndrome, acute respiratory and renal failure, and disseminated intravascular coagulopathy. He died 13 days after birth. Postmortem examination revealed jaundice, anasarca, massive hepatic necrosis, adrenal hemorrhagic necrosis, renal medullary hemorrhage, hemorrhagic noninflammatory pneumonia, and severe encephalomalacia. Echovirus type 6 was isolated from blood, liver, and lungs. Although uncommon, echovirus type 6 infection may produce a spectrum of pathologic findings similar to those seen with the more commonly virulent echovirus type 11. Echoviruses are single-stranded RNA viruses of the genus Enterovirus of the family Picornaviridae that may occasionally cause overwhelming disease and death in neonates (1, 2). Of the 31 types of echoviruses, type 11 is the most frequent cause of serious neonatal morbidity and mortality, often presenting as fulminant hepatitis, infection of the central nervous system, or both (3). Echovirus type 6 infection is an uncommon cause of neonatal mortality, with only a few reported cases of severe or fatal neonatal infection (3-7). We present the case of a newborn infant with fatal echovirus 6 infection and describe the unusual pathologic findings. We also review the literature about severe neonatal echovirus 6 infections. CASE REPORTA full-term boy appropriate for his gestational age was born via caesarian section to a 26-year-old G 1 P 0 Latin American woman who had a medical history of a well-controlled seizure disorder for which she was receiving carbamazepine. She had received regular prenatal care, with negative prenatal serologic tests for human immunodeficiency virus, hepatitis B virus, and syphilis. Two weeks before delivery, she experienced fever and an upper respiratory tract infection. At birth, the infant weighed 3838 g and had an Apgar score of 9. The neonate was put under an oxygen hood, then was later slowly weaned from it. On his fourth day of life, the neonate developed fever (38.6°C) and was observed to have decreased activity. An area of hyperemia and swelling was seen on the right shoulder. This area of swelling and redness increased in size during the next few days. He received ampicillin, gentamicin, ceftazidime, and acyclovir after blood was collected for viral and bacterial cultures. Cranial ultrasonography results were normal.On the fifth day of life, the neonate experienced respiratory difficulty, which required intubation and mechanical ventilation. He remained febrile and developed oliguria that later progressed to renal insufficiency. Sepsis and disseminated intravascular coagulopathy were suspected, and blood and blood products were provided. On the ninth day of life, he suffered cardiopulmonary arrest twice and remained neurologically compromised thereafter. He was transferred to the University of Texas Medical Branch ...
Infectious mononucleosis (IM) due to all causes is characterized by atypical lymphocytosis. We sought to compare hematologic parameters of infectious mononucleosis due to Epstein-Barr virus (EBV) infection (heterophile antibody (HA) positive) with mononucleosis due to other causes. Mono-Latex Slide Agglutination Test results and complete blood counts (CBC) of 147 patients with mononucleosis were retrospectively analyzed. Leukocyte count, absolute lymphocyte count, and presence of atypical lymphocytes in EBV-positive and EBV-negative groups were statistically compared. We analyzed 68 EBV-positive and 79 EBV-negative cases. EBV-positive patients were significantly younger than EBV-negative patients were. Mean total WBC count and mean absolute lymphocyte count were significantly higher in EBV-positive patients. Absolute lymphocytosis, absolute leukocytosis, and atypical lymphocytosis were also significantly more frequent in EBV-positive patients. Leukopenia was more frequently seen in EBV-negative patients. Am.
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