scholarly journals Protracted course of disseminated adenovirus disease with necrotizing granulomas in the liver

2019 ◽  
Vol 94 (2) ◽  
pp. 180-182 ◽  
Author(s):  
Andrea M. Lerner ◽  
John E. Bennett ◽  
Stefania Pittaluga ◽  
Pavel P. Khil ◽  
JH Youn ◽  
...  
2019 ◽  
Vol 114 (1) ◽  
pp. S1171-S1171
Author(s):  
Scott R. Douglas ◽  
Nitisha Lotun ◽  
Danielle Moore ◽  
Amy Doran ◽  
R. Ann Hays

2013 ◽  
Vol 17 (6) ◽  
pp. 377-383 ◽  
Author(s):  
Kristin Noiles ◽  
Katie Beleznay ◽  
Richard I. Crawford ◽  
Sheila Au

Background: Sarcoidosis is a systemic inflammatory disorder with cutaneous involvement present in 25% of cases. The presence of naked granulomas histologically is the hallmark of sarcoidosis. The presence of necrotizing granulomas is highly suggestive of other granulomatous conditions and leads the clinician to pursue other diagnoses, such as infectious causes. Objectives: We describe two cases of sarcoidosis in which necrotizing granulomas were present on biopsy. Both patients had ulcerated cutaneous lesions of sarcoidosis. In one case, the presence of these atypical histologic features led to a delay in diagnosis of almost 10 years. We review the various histopathologic findings associated with cutaneous sarcoidosis and discuss a potential connection between ulcerated sarcoidosis and atypical histologic findings. Conclusion: When atypical histopathologic features are present, the differential diagnosis of sarcoidosis should not be excluded.


Chest Imaging ◽  
2019 ◽  
pp. 441-446
Author(s):  
Juliana Bueno

Sarcoidosis is a systemic disease of unknown etiology, characterized by noncaseating epithelioid cell granulomas. Patients with sarcoidosis are frequently asymptomatic and may be diagnosed incidentally because of an abnormal imaging study. Sarcoidosis is a diagnosis of exclusion that warrants pathological confirmation in all cases. The distribution of granulomas in the lungs is characteristic and correlates with imaging findings; non-necrotizing granulomas classically exhibit a perilymphatic distribution. On chest radiography, the presence of bilateral hilar and right paratracheal lymphadenopathy, particularly in a young asymptomatic patient, should raise the possibility of sarcoidosis. On CT, a perilymphatic distribution (peribronchovascular, subpleural, septal) of abnormalities in the appropriate clinical context is highly specific for sarcoidosis.


2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Mehmet Akce ◽  
Sarah Bonner ◽  
Eugene Liu ◽  
Rebecca Daniel

A 67-year-old male presented with fatigue, abdominal pain , and 30-pound weight loss over 3 months. Computerized tomography (CT) abdomen displayed ascites with thickening and enhancement of the peritoneum and mottled nodular appearing as soft tissue consistent with omental caking worrisome for peritoneal carcinomatosis. A paracentesis revealed white blood cell count of 2,500 with 98% lymphocytes and serum ascites albumin gradient of 0.9 g/L. No acid-fast bacilli were seen by microscopic exam and culture was negative. Purified protein derivative skin test (PPD) was negative and CXR did not reveal any infiltrates. Esophagogastroduodenoscopy (EGD) and colonoscopy were unrevealing. The patient underwent exploratory laparotomy with round ligament and peritoneal biopsies that revealed numerous necrotizing granulomas. Acid-fast bacteria Ziehl-Neelsen stain (AFB) of the biopsy specimen revealed single acid-fast bacilli. Treatment for M. tuberculosis was initiated and final culture revealed that mycobacterium tuberculosis was sensitive to Isoniazid, Rifampin, Ethambutol, and Pyrazinamide. After 6 months of treatment, the ascites and peritoneal carcinomatosis resolved.


Pathobiology ◽  
2018 ◽  
Vol 85 (5-6) ◽  
pp. 276-279 ◽  
Author(s):  
Elena Bargagli ◽  
Paola Rottoli ◽  
Elena Torricelli ◽  
Chiara Allegrini ◽  
Alessandra Dubini ◽  
...  

Aorta ◽  
2016 ◽  
Vol 04 (01) ◽  
pp. 25-28
Author(s):  
Sarah-Jayne Edmondson ◽  
Saina Attaran ◽  
Ulrich Rosendahl

AbstractWegner’s granulomatosis (WG) is an autoimmune systemic vasculitis that results in necrotizing granulomas. We report a WG patient with a lung granuloma and aortic root dilatation, who underwent aortic root replacement on cardiopulmonary bypass (CPB). Intraoperatively, the patient suffered an aortic dissection, which was repaired immediately under deep hypothermic circulatory arrest (DHCA). Follow-up imaging showed complete granuloma resolution, despite absence of immunosuppressive therapy. Immune stimulation following CPB is well described; here, the opposite was observed and DHCA effects are discussed.


2019 ◽  
Vol 31 (6) ◽  
pp. 844-851
Author(s):  
Mitchell V. Palmer ◽  
Carly Kanipe ◽  
Rebecca Cox ◽  
Suelee Robbe-Austerman ◽  
Tyler C. Thacker

Paratuberculosis (Johne’s disease) is caused by Mycobacterium avium ssp. paratuberculosis (MAP), and affects both domestic and wild ruminants, including cattle, goats, sheep, and deer. In cattle, most infections occur during calfhood followed by a prolonged incubation period of 1–2 y or more before cows shed culturable numbers of MAP bacilli in their feces. As disease progresses, infected animals develop protein-losing enteropathy, intractable diarrhea, and weight loss. In a cohort of 32 clinically normal deer from a herd with a history of periodic clinical paratuberculosis, we found that subclinical infection was characterized by high rates of infection, common involvement of mesenteric lymph nodes, minimal lesion formation, few intralesional acid-fast bacilli, and low-level fecal shedding of MAP. The characteristics of subclinical paratuberculosis in white-tailed deer resemble those of cattle and red deer, although microscopic lesions were less common in subclinical deer than reported for subclinical cattle, and we did not see necrotizing granulomas as described in subclinical red deer and elk.


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