Zahed Ali Qamer,Monika Maharjan,Kranthi Kumar Jandrasupalli et al.
Zahed Ali Qamer et al.
Melanoma arising in the hard palate is an exceedingly rare entity, comprising a minute fraction of all melanoma cases. The absence of specific clinical signs often leads to delayed diagnosis and subsequent challenges in treatment planning. ...
Gallbladder schistosomiasis [0.03%]
胆囊血吸虫病
Gabriela Del Angel-Millán,José Jukemura,Júlia Bragion Bicudo et al.
Gabriela Del Angel-Millán et al.
Schistosomiasis is an infectious disease caused by parasitic flatworms of the genus Schistosoma. The species Schistosoma mansoni is associated with hepatosplenic disease. Schistosomiasis involving the gallbladder alone is highly unusual, wi...
Case Reports
Autopsy & case reports. 2024 Oct 8:14:e2024516. DOI:10.4322/acr.2024.516 2024
Explant pathology in Biliary Atresia post Kasai procedure: a tale of two livers [0.03%]
Kasai术后胆道闭锁患儿肝移植 explant病理：两种结局
Sunayana Misra,Sonia Badwal,Shashi Dhawan et al.
Sunayana Misra et al.
Biliary atresia (BA) is a progressive inflammatory cholangiopathy of infancy that results in fibrous obliteration of the extrahepatic and intrahepatic bile ducts. In untreated patients, this leads to biliary-type cirrhosis within the first ...
Case Reports
Autopsy & case reports. 2024 Oct 8:14:e2024521. DOI:10.4322/acr.2024.521 2024
Multicystic encephalopathy: an ultimate manifestation of ischemic-hypoxic injury [0.03%]
多囊性脑病：缺血-缺氧性损伤的最终表现形式
Vielka Fernandez Aragones,Amilcar Castellano-Sanchez,Gabriel Chamyan et al.
Vielka Fernandez Aragones et al.
Multicystic encephalopathy is a rare neurological finding characterized by the appearance of multiple cystic or cavitary lesions as the result of repetitive episodes of hypoxic-ischemic injury in neonates and infants. We present a rare case...
Anti MDA-5 associated rapidly progressive interstitial lung disease complicated by viral pneumonia - a fatal outcome [0.03%]
抗MDA-5抗体阳性快速进展性间质性肺病合并病毒性肺炎1例及其预后因素分析
Saikat Mitra,Nithye Parvathy,Mandeep Garg et al.
Saikat Mitra et al.
Dermatomyositis is a heterogeneous systemic disease, with 7% to 10% of the individuals presenting the Anti MDA-5 antibody. This subset of patients has clinically amyotropic dermatomyositis, presenting with cutaneous ulcer and rapidly progre...
Systemic amyloidosis: an aggressive evolution in a patient with relapsing polychondritis and monoclonal gammopathy of undetermined significance (MGUS) undergoing peritoneal dialysis [0.03%]
系统性淀粉样变性：腹膜透析患者合并复发性多软骨炎和意义未明的单克隆免疫球蛋白血症（MGUS）的病情进展病例报告
Thiago Cavalcanti Matos,William George Giusti Fischer,Rosa Maria Rodrigues Pereira et al.
Thiago Cavalcanti Matos et al.
Herein, we report the case of primary amyloidosis with multi-organ involvement in a female patient in her 50s. The patient had a history of relapsing polychondritis, chronic kidney disease, and monoclonal gammopathy of undetermined signific...
Ravi Hari Phulware,Kaashvi Gupta,Gaurav Rajendra Shirsath et al.
Ravi Hari Phulware et al.
Mönckeberg calcified sclerosis preventing the use of radial artery in myocardial revascularization surgery [0.03%]
Mönckeberg动脉钙化硬化症对桡动脉在冠状动脉旁路移植术中应用的影响
Luiz Alberto Benvenuti
Luiz Alberto Benvenuti
Saikat Mitra,Shouvanik Satpathy,Devmalya Banerjee et al.
Saikat Mitra et al.
Atypical parathyroid tumor (APT) is a rare neoplasm of the parathyroid gland, which shows atypical cytological or architectural features and lacks definite diagnosis criteria for malignancy. These cases can cause diagnostic challenges owing...
Deepa Rani,Anupam Varshney,Kanika Rastogi
Deepa Rani
Castleman disease (CD) is a rare, benign lymphoproliferative disorder, mostly involving the mediastinal lymph nodes, but can occur wherever lymphoid tissue is found. With only a few published case reports, there needs to be more literature ...