Eosinophilic esophagitis is a rare disease in Asian countries, but its incidence is growing rapidly in Western countries. The main pathophysiology of eosinophilic esophagitis is esophageal epithelial barrier dysfunction; disruption of the esophageal epithelial barrier easily induces antigen sensitization to foods and aeroallergens, which leads to subsequent esophageal inflammation as a result of eosinophil recruitment. Here we report a case of an 11-year-old Korean boy who suffered from fever, odynophagia, dysphagia, and chest pain. His upper endoscopic findings showed longitudinal ulcers with a volcano-like appearance at the distal esophagus. Polymerase chain reaction test results and biopsy specimens were positive for herpes simplex virus type 1. He was treated with acyclovir and a proton pump inhibitor, but his follow-up endoscopy showed typical patterns of eosinophilic esophagitis, and the biopsy specimens were compatible with the diagnostic criteria for eosinophilic esophagitis. Therefore, we report a very rare case of eosinophilic esophagitis after herpes esophagitis in a Korean child with normal immunity.
Acyclovir ; Asian Continental Ancestry Group ; Biopsy ; Chest Pain ; Child ; Deglutition Disorders ; Endoscopy ; Eosinophilic Esophagitis ; Eosinophils ; Esophagitis ; Esophagus ; Fever ; Follow-Up Studies ; Herpesvirus 1, Human ; Humans ; Incidence ; Inflammation ; Male ; Polymerase Chain Reaction ; Proton Pumps ; Rare Diseases ; Simplexvirus ; Ulcer

Anaplastic transformation of differentiated thyroid cancer at distant metastatic sites is extremely rare and has a poor prognosis. It usually occurs in the thyroid gland or cervical lymph nodes. Here we report a case of anaplastic transformation arising at multiple distant metastatic sites including the lung, liver, adrenal gland, bone, and lymph nodes in a patient 3 years after total thyroidectomy for follicular thyroid cancer.
Adrenal Glands* ; Humans ; Liver* ; Lung* ; Lymph Nodes ; Prognosis ; Thyroid Gland* ; Thyroid Neoplasms* ; Thyroidectomy

Calcitonin is an important tumor marker for medullary thyroid carcinoma. Serum calcitonin is increased in most cases of medullary thyroid carcinoma. However, medullary thyroid carcinoma with normal calcitonin level has been reported very rarely. 1.2 cm sized solid thyroid nodule was suspicious for medullary thyroid carcinoma in fine needle aspiration cytology, but serum calcitonin was within the normal range. The final pathology after surgery was medullary thyroid carcinoma with positive calcitonin immunohistochemical staining. The authors present a case of calcitonin-negative medullary thyroid cancer with reviews of the mechanism, diagnosis, treatment, prognosis and follow-up of this case.

Calcitonin is an important tumor marker for medullary thyroid carcinoma. Serum calcitonin is increased in most cases of medullary thyroid carcinoma. However, medullary thyroid carcinoma with normal calcitonin level has been reported very rarely. 1.2 cm sized solid thyroid nodule was suspicious for medullary thyroid carcinoma in fine needle aspiration cytology, but serum calcitonin was within the normal range. The final pathology after surgery was medullary thyroid carcinoma with positive calcitonin immunohistochemical staining. The authors present a case of calcitonin-negative medullary thyroid cancer with reviews of the mechanism, diagnosis, treatment, prognosis and follow-up of this case.

Calcitonin is an important tumor marker for medullary thyroid carcinoma. Serum calcitonin is increased in most cases of medullary thyroid carcinoma. However, medullary thyroid carcinoma with normal calcitonin level has been reported very rarely. 1.2 cm sized solid thyroid nodule was suspicious for medullary thyroid carcinoma in fine needle aspiration cytology, but serum calcitonin was within the normal range. The final pathology after surgery was medullary thyroid carcinoma with positive calcitonin immunohistochemical staining. The authors present a case of calcitonin-negative medullary thyroid cancer with reviews of the mechanism, diagnosis, treatment, prognosis and follow-up of this case.

Oral spindle cell/sclerosing rhabdomyosarcoma (SCRMS) with anaplastic lymphoma kinase (ALK) expression is extremely rare, and its diagnosis is very challenging in the absence of clinical or pathological indicators. This case presented with gingival swelling and alveolar bone resorption and was suspected clinically to be periodontitis. A biopsy was performed and, due to immunoreactivity with ALK, the patient was misdiagnosed with inflammatory myofibroblastic tumor. However, based on the combined histological and immunohistochemical features, a revised diagnosis of SCRMS with ALK expression was finally concluded. We believe that this report makes a significant contribution to the precise diagnosis of this rare disease for proper treatment.

Anaplastic thyroid carcinoma (ATC) is an uncommon aggressive malignant tumor, and the osteoclastic variant of ATC is extremely rare. We report here on the fine needle aspiration cytology of the osteoclastic variant of ATC in an 83-year-old woman. The smear was composed of many oval to slightly elongated undifferentiated mononuclear cells admixed with multinucleated osteoclast-like giant cells. The mononuclear tumor cells revealed inconspicuous nuclear pleomorphism and the nuclei were characterized by vesicular chromatin and an indented or lobulated nuclear membrane with conspicuous nuclear grooves. A few epithelial clusters suggestive of a papillary carcinoma component were also observed. Making the proper cytological diagnosis of the osteoclastic variant of ATC is helpful to determine the proper treatment modality for these patients.
Aged, 80 and over ; Anaplasia ; Biopsy, Fine-Needle ; Carcinoma, Papillary ; Chromatin ; Female ; Giant Cells ; Humans ; Nuclear Envelope ; Osteoclasts ; Thyroid Gland ; Thyroid Neoplasms

BACKGROUND: Although Kikuchi's lymphadenitis (KL) has been known to have characteristic cytological features, pathologists encounter difficulties in making a diagnosis with fine needle aspiration cytology (FNAC). The objective of this study was to assess the diagnostic pitfalls of KL with FNAC, particularly with emphasis on differential diagnosis with tuberculosis. METHODS: FNAC of 10 patients with a histological diagnosis of KL and tuberculosis was reviewed. RESULTS: Acidophilic cells were observed in all the 10 KL cases, even if the smears were insufficient. Crescentic histiocytes were seen in 8, granular background in 7, and karyorrhectic debris in 3 cases. Epithelioid histiocytes or neutrophils were not seen in any of the KL cases. Of the 10 cases of tuberculosis, acidophilic cells were observed in 6 cases, crescentic histiocytes in none of them, cheese-like background in 9, karyorrhectic debris in 8, epithelioid histiocytes in 4, and neutrophils in 8 cases. CONCLUSIONS: The acidophilic cell could be the most sensitive but not the specific marker of KL with FNAC. The crescentic histiocytes might be the sensitive and considerably specific marker of KL. The cytological features distinguishing tuberculosis from KL may be cheese-like necrosis admixed with neutrophils and epithelioid histiocytes.
Biopsy, Fine-Needle ; Diagnosis, Differential ; Histiocytes ; Histiocytic Necrotizing Lymphadenitis ; Humans ; Lymphadenitis ; Necrosis ; Neutrophils ; Tuberculosis

BACKGROUND/AIMS: The invasiveness of a liver biopsy and its inconsistent results have prompted efforts to develop noninvasive tools to evaluate the severity of chronic hepatitis. This study was intended to assess the performance of serum biomarkers for predicting liver fibrosis in patients with chronic viral hepatitis. METHODS: A total of 302 patients with chronic hepatitis B or C, who had undergone liver biopsy, were retrospectively enrolled. We investigated the diagnostic accuracy of several clinical factors for predicting advanced fibrosis (F≥3). RESULTS: The study population included 227 patients with chronic hepatitis B, 73 patients with chronic hepatitis C, and 2 patients with co-infection (hepatitis B and C). Histological cirrhosis was identified in 16.2% of the study population. The grade of porto-periportal activity was more correlated with the stage of chronic hepatitis compared with that of lobular activity (r=0.640 vs. r=0.171). Fibrosis stage was correlated with platelet count (r=-0.520), aspartate aminotransferase to platelet ratio index (APRI) (r=0.390), prothrombin time (r=0.376), and albumin (r=-0.357). For the diagnosis of advanced fibrosis, platelet count and APRI were the most predictive variables (AUROC=0.752, and 0.713, respectively). CONCLUSIONS: In a hepatitis B endemic region, platelet count and APRI could be considered as reliable non-invasive markers for predicting fibrosis of chronic viral hepatitis. However, it is necessary to validate the diagnostic accuracy of these markers in another population.
Aspartate Aminotransferases ; Biomarkers* ; Biopsy ; Blood Platelets ; Coinfection ; Diagnosis ; Fibrosis* ; Hepatitis B ; Hepatitis B, Chronic ; Hepatitis C, Chronic ; Hepatitis* ; Hepatitis, Chronic ; Humans ; Liver ; Liver Cirrhosis ; Platelet Count ; Prothrombin Time ; Retrospective Studies

Synovial chondromatosis is a rare metaplastic disease affecting the joints, including the temporomandibular joint (TMJ). Since its symptoms are similar to those of temporomandibular disorders, a careful differential diagnosis is essential. A 50-year-old male patient was referred with the chief complaint of pain and radiopaque masses around the left TMJ on panoramic radiography. Clinically, pre-auricular swelling and resting pain was found, without limitation of mouth opening. On cone-beam computed tomographic images, multiple calcified nodules adjacent to the TMJ and bone proliferation with sclerosis at the articular fossa and eminence were found. T2-weighted magnetic resonance images showed multiple signal-void nodules with high signal effusion in the superior joint space and thickened cortical bone at the articular fossa and eminence. The calcified nodules were removed by surgical excision, but the hypertrophic articular fossa and eminence remained. A histopathological examination confirmed the diagnosis. The patient was followed up few months later without recurrence.
Chondromatosis, Synovial ; Cone-Beam Computed Tomography ; Diagnosis ; Diagnosis, Differential ; Humans ; Joints ; Male ; Middle Aged ; Mouth ; Radiography, Panoramic ; Recurrence ; Sclerosis ; Temporal Bone ; Temporomandibular Joint Disorders ; Temporomandibular Joint