Vol. 12 No. 10 (2025)

Articles

• DOI: 10.12890/2025_005755

  Strawberry gingivitis as the initial manifestation of granulomatosis with polyangiitis in a patient with alpha-1 antitrypsin deficiency

  Ayema Haque, Humza Naveed, Gautam Pandrangi, Laiba Gulzar, Harshank Patel, Vanita Motiani, Satish Solanki

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• DOI: 10.12890/2025_005834

  Gastric melanoma in a 19-year-old patient: a rare case and a review of diagnostic pitfalls

  Jinane Kharmoum, Mohamed El Jiar, Imane Eliahai, Hassan Ouaya, Sanae Chaib, Ihssane Mellouki, Mariame Chraibi

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• DOI: 10.12890/2025_005823

  When new therapies meet old challenges: tirzepatide–warfarin interaction in a mechanical mitral valve patient

  Raffaele Natale, Annadora Morena, Luca Maria Capece, Sofia Donnarumma, Ermenegilda Pagano, Fabrizio Pasanisi, Lidia Santarpia

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• DOI: 10.12890/2025_005818

  Paraspinal extramedullary haematopoiesis in a patient with sickle cell disease: a rare clinical presentation

  Anurag Raje, Gowtham Siddi, Amita D'Souza, Amit Correa

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• DOI: 10.12890/2025_005814

  Serratia marcescens sinusitis presenting as left orbital apex syndrome

  Yusuf Kagzi, Murtaza Khambati, Varshini Thiruvadi, Tulika Chatterjee

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• DOI: 10.12890/2025_005790

  The great mimicker: pulmonary adenocarcinoma with interstitial lung disease-like presentation

  Mahima Upadhyay, Prajwal Shanker, Susheel Joshi, Urooj Khan

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• DOI: 10.12890/2025_005785

  What are the safest and easiest extra-cardiac biopsy sites for the diagnosis of wild-type transthyretin cardiac amyloidosis? Confirmation of the diagnosis by biopsy of the pectoralis muscle during pacemaker insertion

  Koji Takahashi, Mitsuharu Ueda, Yushi Utsunomiya, Hiroe Morioka, Shigeki Uemura, Tomoki Sakaue, Katsuji Inoue

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• DOI: 10.12890/2025_005783

  Uncovering the cause of pneumonia: reactivation of HHV-6B in an immunocompromised patient

  Leonor Rodrigues, Juliana Nogueira, Daniela Alves, Filipa Ferreira, João Fonseca

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• DOI: 10.12890/2025_005779

  Slow evolution of non-familial autoimmune polyglandular syndrome type II in a 54-year-old female, first presenting with Addison’s disease, then Hashimoto’s thyroiditis, which then transitioned to Graves’ disease and then the development of type 1 diabetes

  Ghayda’ E’leimat, Thuy Hao Nguyen, Hemant Thawani

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• DOI: 10.12890/2025_005777

  Cytomegalovirus viremia as a cause of fever of unknown origin in an immunocompetent adult

  Aaron Naveen Joseph, Samuel VanBeck, Nooria Saif, Tahreem Ahmad, Islam Younes

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• DOI: 10.12890/2025_005764

  Guillain-Barré syndrome as the initial clinical manifestation of Hodgkin’s lymphoma

  Vasileios Petrakis, Georgios Tartanis, Soultana Tsakaldimi, Ioulia Dragoumani, Athina Danadaki, Christoforos Roubakis, Christina Aggelopoulou

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• DOI: 10.12890/2025_005762

  Severe leptospirosis with apyrexia and an atypical presentation: rapid progression to multi-organ failure

  Ngoc Anh Doi, Van Thoai Pham, Viet Nghia Le, Quoc Phuong Nguyen

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• DOI: 10.12890/2025_005534

  Langerhans cell histiocytosis successfully treated with combination of thalidomide and corticosteroid

  Nadia Ayu Mulansari, Abdul Muthalib, Cynthia Kurniawan

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• DOI: 10.12890/2025_005754

  Cerebral vein sinus thrombosis, an unusual complication of inflammatory bowel disease

  Ahmad Yehia, Themba Mudege, Sami Hoque

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• DOI: 10.12890/2025_005734

  Spontaneous splenic rupture as an uncommon complication of acute pancreatitis

  Marco Antonio Rodriguez Sanchez, Pedro Nieto, Omar Morales, Airam Lopez, Luis Beltran, Ramon Ruelas, Juan Mendez

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• DOI: 10.12890/2025_005733

  A patient with VEXAS syndrome presenting with complete ophthalmoplegia

  James Krzowski, Luke Harvey, Emily Mitchell, Vivek Rajagopal

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• DOI: 10.12890/2025_005728

  Hypotension-induced transverse spinal cord ischemia

  Peter Kordis, Fuad Colakovic, Eva Pipan

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• DOI: 10.12890/2025_005721

  Higher doses of eculizumab may be beneficial in paroxysmal nocturnal haemoglobinuria in pregnancy

  Harshank Vishnubhai Patel, Steve Stone, Madison C. Laird, Vanita Motiani, Ayema Haque, MBBS, Hemasri Tokala, Akshay Amaraneni

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• DOI: 10.12890/2025_005706

  A very rare SETX gene variant (c.2750T>C) in a 72-year-old man with amyotrophic lateral sclerosis and an unremarkable family history. Should genetic testing be routinely performed in all patients?

  Andreas Posa, Malte Kornhuber

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• DOI: 10.12890/2025_005699

  Supraventricular tachycardia in a young adult with congenital heart disease: successful ablation after patent ductus arteriosus closure

  Bunga Bella Pratiwi, Ardian Rizal, Valerinna Yogibuana

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• DOI: 10.12890/2025_005677

  Respiratory-predominant relapsing polychondritis: the role of PET scan in making this challenging diagnosis

  Daniela Alves, João Fonseca, Miguel Martins, Valter Duarte, Gisela Gonçalves, Pedro Lopes

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• DOI: 10.12890/2025_005636

  An unusual case of tinzaparin-induced haemorrhagic bullous dermatosis: diagnostic and therapeutic challenges

  Khadidja Abdelhamid, Guillaume Chaby, Marine Serpier-Vangheluwe, Jean Schmidt, Valery Salle

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• DOI: 10.12890/2025_005625

  Nivolumab-induced chylothorax in a patient with advanced gastric adenocarcinoma

  Youssef Hayssam Sultan, Radwan Zeidan, Mohammed Abdallah, Staphanie Joseph Mitri, Francois Georges Kamar

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