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Background: Peripheral T cell lymphoma (PTCL), not otherwise specified (NOS) is a heterogenous group of predominantly nodal T cell lymphomas that generally presents with lymphadenopathy with or without extra nodal involvement. Acral vascular syndrome clinically presents as digital ischemia with Raynaud's phenomenon and acral cyanosis. Although, this condition is commonly associated with connective tissue disorder, smoking and vasculitis, its association with lymphoid malignancy is very rare. Here, we present a case report of a patient with digital gangrene of all toes and fingers as a presenting symptom of PTCL-NOS.
Case Description: A 62 year old male presented with digital ischemia associated with pain, low grade fever, loss of appetite and significant weight loss of 6 kilograms over a period of 3 months. On examination, he was found to have bilateral inguinal and axillary lymph nodes with gangrenous changes over toes and fingers but peripheral pulses were palpable. On evaluation he had anemia, elevated ESR and CRP. CT angiogram revealed thinned out digital arteries with multifocal areas of narrowing. Patient was screened for other causes of digital gangrene and was tested negative for ANCA, ANA, cryoglobulins and viral markers. Lymph node biopsy with IHC was suggestive of peripheral T-cell lymphoma-NOS and was started on CHOP regimen. Lymph nodes size decreased and gangrenous changes resolved.
Conclusion: Though digital ischemia is a rare paraneoplastic presentation of lymphoma, it should be considered if there is a rapid progression of gangrene. Early initiation of chemotherapy may result in the reduction of further progression of digital gangrene and thus prevent permanent disability. In our patient, progression of gangrene was prevented even though it was an aggressive variant of T cell lymphoma.
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http://dx.doi.org/10.59556/japi.71.0370 | DOI Listing |
BMJ Case Rep
August 2025
Internal Medicine, Parc Taulí Hospital Universitari, Sabadell, Spain.
Paraneoplastic acral vascular syndrome (PAVS) is a rare condition characterised by signs of digital ischaemia, including Raynaud's phenomenon, acrocyanosis and digital gangrene, in the context of an underlying neoplastic process. Prompt recognition of this syndrome, as well as accurate identification and classification of the associated neoplastic condition, are crucial.This report describes the case of a woman diagnosed with PAVS secondary to stage IV non-small cell lung adenocarcinoma harbouring a Kirsten Rat Sarcoma viral homolog oncogene (KRAS) G12A mutation (p.
View Article and Find Full Text PDFCureus
July 2025
General Pediatrics, Al Jalila Children's Speciality Hospital, Dubai, ARE.
Infective endocarditis (IE) is a rare but life-threatening condition in children, particularly in those without heart disease. Delayed diagnosis can lead to serious systemic complications. We report the case of an eight-year-old previously healthy girl, initially misdiagnosed with bacterial meningitis, who developed multiple septic embolic events (cerebral infarcts, digital gangrene, and splenic and renal infarction) despite being on antibiotic therapy.
View Article and Find Full Text PDFAm J Case Rep
July 2025
Department of Surgery, Mayo Clinic Health System, Eau Claire, WI, USA.
BACKGROUND Intra-thoracic bleeding in the form of hemo-mediastinum is a rare condition often resulting from trauma or malignancy, or can occur spontaneously. Spontaneous intra-thoracic bleeding, particularly following laparoscopic appendectomy, is extremely uncommon and not typically associated with such procedures. CASE REPORT A 65-year-old man with a history of interstitial lung disease due to mixed connective tissue disease, chronic cough, pleurodesis, and coronary artery disease developed massive mediastinal hematoma and hemodynamic instability following an uncomplicated laparoscopic appendectomy for gangrenous appendicitis.
View Article and Find Full Text PDFBMJ Case Rep
July 2025
Department of Surgical Discipline, All India Institute of Medical Sciences Bathinda, Bathinda, Punjab, India.
A man in his 60s presented with severe abdominal pain, vomiting and obstipation for the last 2 days. His examination revealed a tender abdomen. The contrast-enhanced CT of the abdomen reported superior mesenteric artery thrombosis with ischaemic changes in the bowel.
View Article and Find Full Text PDFMod Rheumatol Case Rep
July 2025
Department of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Dermatomyositis (DM) is an idiopathic inflammatory myopathy with characteristic cutaneous manifestations and systemic complications, including malignancy and interstitial lung disease (ILD). Myositis-specific autoantibodies (MSAs) define distinct disease subtypes, but significant clinical heterogeneity can still occur. Here, we report a unique case of smouldering myeloma-associated anti-nuclear matrix protein 2 (anti-NXP2) antibody-positive DM mimicking clinical features of anti-melanoma differentiation-associated gene 5 (anti-MDA5) antibody-positive DM, including digital ischemia and palmar papules (i.
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